@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y> .
@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:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_head {
  this: np:hasAssertion dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_assertion;
    np:hasProvenance dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_provenance;
    np:hasPublicationInfo dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_assertion a np:Assertion .
  
  dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_provenance a np:Provenance .
  
  dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_assertion {
  miriam-gene:3082 a ncit:C16612 .
  
  lld:C0039101 a ncit:C7057 .
  
  dgn-gda:DGNe1117fdc134ea5136e813f2d0238155b sio:SIO_000628 miriam-gene:3082, lld:C0039101;
    a sio:SIO_001121 .
}

dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_provenance {
  dgn-np:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_assertion dcterms:description
      "[These results suggest that the sustained phosphorylation of Gab1 through Crk in response to HGF contributes to the prominent activation of Rac1 leading to enhanced cell motility, scattering, and cell invasion, which may support the crucial role of Crk in the aggressiveness of human synovial sarcoma.]. 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:16849525;
    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:NP169477.RADhiy-r1K5wMKfGTxPnYl9_fOG7HLg3rWsosV2SdzC0Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:31+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" .
}