@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc> .
@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:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_head {
  this: np:hasAssertion dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_assertion;
    np:hasProvenance dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_provenance;
    np:hasPublicationInfo dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_assertion a np:Assertion .
  
  dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_provenance a np:Provenance .
  
  dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_assertion {
  miriam-gene:8731 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNde0e4c664193361d5ac060fc342600a0 sio:SIO_000628 miriam-gene:8731, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_provenance {
  dgn-np:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_assertion dcterms:description
      "[The observed spectrum of mutations in resistant cells was dominated by substitutions of tyrosine 1230 but also included other missense mutations and partially overlapped with activating MET mutations that were previously described in cancer patients.]. 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:21697284;
    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:NP160444.RAf3qT3UxMbmycIe8vImm_nt_qR9TDg4SBpT8RikB-Fgc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}