@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE> .
@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:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_head {
  this: np:hasAssertion dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_assertion;
    np:hasProvenance dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_provenance;
    np:hasPublicationInfo dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_assertion a np:Assertion .
  
  dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_provenance a np:Provenance .
  
  dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_assertion {
  miriam-gene:9628 a ncit:C16612 .
  
  lld:C0028860 a ncit:C7057 .
  
  dgn-gda:DGN93f800689186cb389409606c4c74e868 sio:SIO_000628 miriam-gene:9628, lld:C0028860;
    a sio:SIO_001121 .
}

dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_provenance {
  dgn-np:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_assertion dcterms:description
      "[The OCRL1 RhoGAP domain showed low Rac GAP activity in vitro, and when expressed in Swiss 3T3 cells induced specific inhibition of RacGTP dependent ruffles, consistent with OCRL1 being an active RacGAP.]. 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:12915445;
    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:NP636168.RAkuQNADeHd9GfT4MZJPpLgJ9N4ietJE4rsdN6gLc85EE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:23+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" .
}