@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI> .
@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/v4.0.0/void/> .
dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_head {
   this: np:hasAssertion dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_assertion ;
    np:hasProvenance dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_provenance ;
    np:hasPublicationInfo dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_assertion a np:Assertion .
  dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_provenance a np:Provenance .
  dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_assertion {
   miriam-gene:7157 a ncit:C16612 .
  lld:C2239176 a ncit:C7057 .
  dgn-gda:DGN7d060e84698547746a3b59fba344f2f4 sio:SIO_000628 miriam-gene:7157 , lld:C2239176 ;
    a sio:SIO_001121 .
}
dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_provenance {
   dgn-np:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_assertion dcterms:description "[β-catenin and P53 mutations represent the two main genetic alterations described in HCC, and P53 and KRAS mutations in CC, but rare genetic alterations could be particularly valuable if they constitute drug-able targets (such as PIK3CA or EGFR mutations).]. 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:21538283 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP891344.RAO5KTIAUlMy7trDLfMM_dvBivwVHk3X_41VnwFYbcrlI130_publicationInfo {
   this: dcterms:created "2016-05-13T12:48:28+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}