@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg> .
@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/v3.0.0/void/> .
dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_head {
  this: np:hasAssertion dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_assertion ;
    np:hasProvenance dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_provenance ;
    np:hasPublicationInfo dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_assertion a np:Assertion .
  dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_provenance a np:Provenance .
  dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_assertion {
  miriam-gene:3082 a ncit:C16612 .
  lld:C0238461 a ncit:C7057 .
  dgn-gda:DGN31ee64a3a4181cc072ac7dbf67dfde00 sio:SIO_000628 miriam-gene:3082 , lld:C0238461 ;
    a sio:SIO_001121 .
}
dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_provenance {
  dgn-np:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_assertion dcterms:description "[Because 1) HGF and c-met map to chromosome 7q21 and 7q31, respectively, 2) FTC loses genetic material at multiple loci with a frequency much higher than PTC, and 3) loss of heterozygosity (LOH) on 7q has been previously found in various tumors, we tested the hypothesis that both FTC and ATC, but not PTC, could harbor LOH in segments of 7q encompassing the loci for HGF and c-met.]. 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:10487693 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP448071.RA_qxPk6-C_GQ0qiJsihrbGJLkCNGLCW7hMt-QSLAnblg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:02+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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}