@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU> .
@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:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_head {
  this: np:hasAssertion dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion ;
    np:hasProvenance dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance ;
    np:hasPublicationInfo dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion a np:Assertion .
  dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance a np:Provenance .
  dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion {
  miriam-gene:138804 a ncit:C16612 .
  lld:C0686619 a ncit:C7057 .
  dgn-gda:DGNb25c5b9195a1cb19b22ef2ae7d264501 sio:SIO_000628 miriam-gene:138804 , lld:C0686619 ;
    a sio:SIO_001121 .
}
dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_provenance {
  dgn-np:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_assertion dcterms:description "[When restricting the analysis to the subset of 38 patients who had molecular testing performed preoperatively on FNAB, the PPV and NPV of BRAF positivity for CLNM was 47 and 91%, respectively, and BRAF positivity was still a significant predictor of CLNM on both univariate (OR 8.4, p=0.01) and multivariate (OR 9.7, p=0.02) analyses.]. 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:22941165 ;
    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:NP922991.RAMwqluAR8K4djDS6JvLrbCpNPVCs2s1Wt3iC1rdcP-sU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:26+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" .
}