@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_head {
  this: np:hasAssertion dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_assertion;
    np:hasProvenance dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_provenance;
    np:hasPublicationInfo dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_assertion a np:Assertion .
  
  dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_provenance a np:Provenance .
  
  dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  
  lld:C0034341 a ncit:C7057 .
  
  dgn-gda:DGNc09566a9d324fb875af6d73425ad7f1d sio:SIO_000628 miriam-gene:5660, lld:C0034341;
    a sio:SIO_001121 .
}

dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_provenance {
  dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_assertion dcterms:description
      "[Using a strategy combining polymerase chain reaction amplification of selected gene fragments, denaturing gradient gel electrophoresis of the amplification products, and direct sequencing of fragments with altered melting behavior, we studied the PC gene exons and exon/intron junctions of subjects with hereditary type I PC deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:1301959;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP333068.RAYJqKeXEE9Ota1Xq98t400OInKXdS2eAmK4OYiWM5HJ0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:16+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}