@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_head {
  this: np:hasAssertion dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion;
    np:hasProvenance dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance;
    np:hasPublicationInfo dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion a np:Assertion .
  
  dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance a np:Provenance .
  
  dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion {
  miriam-gene:2661 a ncit:C16612 .
  
  lld:C0032460 a ncit:C7057 .
  
  dgn-gda:DGN01bec970d15c954f80bdf49fafceed98 sio:SIO_000628 miriam-gene:2661, lld:C0032460;
    a sio:SIO_001121 .
}

dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_provenance {
  dgn-np:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_assertion dcterms:description
      "[Fourteen mutations in human (h) GDF9 have been reported in women with premature ovarian failure or polycystic ovarian syndrome as well as in mothers of dizygotic twins, implicating GDF9 in the etiology of these conditions.]. 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:24438375;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP422200.RAorcH-gAHelJSXRueVP3ulx8YsK5TTnQLm8nje609Clo130_publicationInfo {
  this: dcterms:created "2015-08-25T14:41:45+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}