@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk> .
@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:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_head {
  this: np:hasAssertion dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_assertion ;
    np:hasProvenance dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_provenance ;
    np:hasPublicationInfo dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_assertion a np:Assertion .
  dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_provenance a np:Provenance .
  dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_assertion {
  miriam-gene:3082 a ncit:C16612 .
  lld:C1140680 a ncit:C7057 .
  dgn-gda:DGN8da3d762913f7e7239f7a80dcb2981bd sio:SIO_000628 miriam-gene:3082 , lld:C1140680 ;
    a sio:SIO_001121 .
}
dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_provenance {
  dgn-np:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_assertion dcterms:description "[Since autocrine regulation of HGF-Met is implicated in many forms of human cancer, we investigated whether the predisposition to develop ovarian cancer in women with hereditary ovarian cancer syndromes involves changes in the expression of HGF-Met by the tissue of origin of epithelial ovarian cancers, the ovarian surface epithelium (OSE).]. 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:11313876 ;
    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:NP611903.RANX7lWRnXCMOT2M8HWJW-vdmMMwbigJP1m6KtiYEAwqk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}