#!/usr/bin/perl
=head1 NAME

biblio-soap-example.pl

=head1 SYNOPSIS

Script showing code that uses Bio::Biblio, with 'soap' at OpenBQS.

As of Bioperl version 1.4 there are 3 bibliographic repositories,
stipulated by the -access argument: soap, eutils, and biofetch.
The default is 'soap'. Not all of these repositories support all
the Biblio methods nor are the contents of these repositories
necessarily the same. Choose wisely!

=cut

use strict;
use Bio::Biblio;
use Bio::Biblio::IO;
use Data::Dumper;

# number of articles in 'soap' with author Osborne...
my $num = new Bio::Biblio->find("Osborne","authors")->
  get_count;

# number of articles in OpenBQS with 'topoisomerase' in the title, year 2000,
# ("J Biol Chem","journal") is another example query
$num = new Bio::Biblio->find("topoisomerase","title")->
  find("2000","year")->get_count;

# a reference as XML...
my $xml = new Bio::Biblio->get_by_id("3047008");

# get a reference to an array of ids...
my $arr_ref = new Bio::Biblio->find ("Osborne","authors")->
  find("2000","year")->get_all_ids;

# get the vocabulary of a specific repository, but not all repositories
# support these methods as of Bioperl 1.4...
my $biblio = Bio::Biblio->new(-access => "soap");
my $biblio_ref = $biblio->get_vocabulary_names;
my $val_ref = $biblio->get_all_values('MEDLINE2004/JournalArticle/properties');

# retrieve the entry as text or retrieve specific text fields...
my $medline_id = "88329717";
my $ref = Bio::Biblio->new(-access => "soap")->get_by_id($medline_id);
my $io = Bio::Biblio::IO->new( -result => "raw",
			       -data   => $ref );
my $nextref = $io->next_bibref;
# print the entire hash...
my $dump = Data::Dumper->Dump([$nextref],["$medline_id"]);
# or just the abstract...
my $abstract = $nextref->{article}->{abstract}->{abstractText};
# some hash references are stored in arrays
foreach my $ref ( @{$nextref->{article}->{authors}} ) {
   foreach my $val (values %{$ref}) {
      print $val->{lastName}," ",$val->{initials},"\n";
   }
}
# a few more values
my $year = $nextref->{article}->{journal}->{journalIssue}->{pubDate}->{year};
my $title = $nextref->{article}->{articleTitle};

# put it all together...
my $refs = new Bio::Biblio->find("Osborne","authors")->find("2000","year");
while ($refs->has_next){
   my $ref = $refs->get_next;
   my $io = Bio::Biblio::IO->new( -result => "raw", -data => $ref );
   my $nextref = $io->next_bibref;
   my $abstract = $nextref->{article}->{abstract}->{abstractText};
   # you could also write:
   # my $abstract = Bio::Biblio::IO->new( -result => "raw",
   #  -data => $refs->get_next )->next_bibref->{article}->{abstract}->{abstractText};
   print $abstract,"\n";
}

=head1 Output from Data::Dumper->Dump:

88329717 = {
	    'chemicals' => [
			    {
			     'nameOfSubstance' => 'DNA, Fungal',
			     'registryNumber'  => '0'
			    },
			    {
			     'nameOfSubstance' => 'DNA, Superhelical',
			     'registryNumber'  => '0'
			    },
			    {
			     'nameOfSubstance' => 'RNA Polymerase II',
			     'registryNumber'  => 'EC 2.7.7.-'
			    }
			   ],
	    'journalInfo' => {
			      'medlineTA'   => 'Genes Dev',
			      'country'     => 'UNITED STATES',
			      'nlmUniqueID' => '8711660'
			     },
	    'PMID'      => '3047008',
	    'medlineID' => '88329717',
	    'status'    => 'Completed',
	    'article'   => {
			    'journal' => {
					  'journalIssue' => {
							     'volume'       => '2',
							     'issue'        => '6',
							     'pubDate'      => {
										'month' => 'Jun',
										'year'  => '1988'
									       }
							    },
					  'iSSN' => '0890-9369'
					 },
			    'grants' => [
					 {
					  'agency'  => 'NIGMS',
					  'grantID' => '5R01 GM30454-05',
					  'acronym' => 'GM'
					 }
					],
			    'pagination' => {
					     'medlinePgn' => '766-72'
					    },
			    'abstract' => {
					   'abstractText' => 'We show that induction of transcription of a CYC1-lacZ fusion gene, borne on a yeast plasmid, causes an increase in negative superhelicity of approximately five turns. This increase is abolished by deletion of either essential element of the CYC1 promoter, the upstream activation site (UAS), or the TATA boxes. Several experiments indicate that the size of the increase is proportional to the size of the transcribed region. First, an internal deletion removing half of the CYC1-lacZ transcribed region results in a plasmid whose negative superhelicity on induction is intermediate between promoter-deletion plasmids and the parental plasmid. Second, plasmids bearing insertions of a fragment containing the putative CYC1 terminator into the CYC1-lacZ fusion gene have relative negative superhelicities proportional to the length of the truncated fusion transcripts generated. A plausible model explaining these observations is that local unwinding of the double helix by transcribing RNA polymerase generates positively supercoiled DNA, which is subsequently relaxed by a topoisomerase.'
					  },
			    'languages' => [
					    'eng'
					   ],
			    'publicationTypes' => [
						   'Journal Article'
						  ],
			    'authors' => [
					  {
					   'personalName' => {
							      'initials' => 'BI',
							      'lastName' => 'Osborne',
							      'foreName' => 'B I',
							      'type'     => 'PersonalName'
							     }
					  },
					  {
					   'personalName' => {
							      'initials' => 'L',
							      'lastName' => 'Guarente',
							      'foreName' => 'L',
							      'type'     => 'PersonalName'
							     }
					  }
					 ],
			    'articleTitle' => 'Transcription by RNA polymerase II induces changes of DNA topology in yeast.',
			    'affiliation' => 'Massachusetts Institute of Technology, Department of Biology, Cambridge 02139.'
                           },
	    'dateRevised' => {
			      'day' => '18',
			      'month' => '12',
			      'year' => '2000'
			     },
	    'meshHeadings' => [
			       {
				'descriptorName' => 'Chromosome Deletion'
			       },
			       {
				'descriptorName' => 'DNA, Fungal',
				'subHeadings' => [
						  {
						   'subHeading' => 'genetics',
						   'majorTopic' => 'Y'
						  },
						  {
						   'subHeading' => 'ultrastructure'
						  }
						 ]
			       },
			       {
				'descriptorName' => 'DNA, Superhelical',
				'subHeadings' => [
						  {
						   'subHeading' => 'genetics'
						  }
						 ]
			       },
			       {
				'descriptorName' => 'Genes, Fungal'
			       },
			       {
				'descriptorName' => 'Promoter Regions (Genetics)'
			       },
			       {
				'descriptorName' => 'RNA Polymerase II',
				'subHeadings' => [
						  {
						   'subHeading' => 'metabolism',
						   'majorTopic' => 'Y'
						  }
						 ]
			       },
			       {
				'descriptorName' => 'Saccharomyces cerevisiae',
				'subHeadings' => [
						  {
						   'subHeading' => 'genetics',
						   'majorTopic' => 'Y'
						  }
						 ]
			       },
			       {
				'descriptorName' => 'Support, Non-U.S. Gov\'t'
			       },
			       {
				'descriptorName' => 'Support, U.S. Gov\'t, P.H.S.'
			       },
			       {
				'descriptorName' => 'Transcription, Genetic'
			       }
			      ],
	    'dateCreated' => {
			      'day' => '24',
			      'month' => '10',
			      'year' => '1988'
			     },
	    'citationSubsets' => [
				  'IM'
				 ],
	    'type' => 'MedlineCitation',
	    'dateCompleted' => {
				'day' => '24',
				'month' => '10',
				'year' => '1988'
			       }
	   };

=cut