@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk> .
@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:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_head {
  this: np:hasAssertion dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion ;
    np:hasProvenance dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance ;
    np:hasPublicationInfo dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion a np:Assertion .
  dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance a np:Provenance .
  dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion {
  miriam-gene:5921 a ncit:C16612 .
  lld:C0007097 a ncit:C7057 .
  dgn-gda:DGNf118e7f69f8237597ece2cb0c2ab2eb4 sio:SIO_000628 miriam-gene:5921 , lld:C0007097 ;
    a sio:SIO_001121 .
}
dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_provenance {
  dgn-np:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_assertion dcterms:description "[While for most human solid tumors genetic alterations of few distinct genetic regions have been found, studies on basal cell carcinomas (BCC) have shown the prevalence of several abnormalities including alterations of the three ras genes, GAP (GTPase activating protein), p53, PTCH (the human homologue of Drosophila patched) and SMOH (the human homologue of Drosophila smoothened).]. 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:11752813 ;
    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:NP774110.RA519XYIKDdAB66A0_2VB_tHc0GihULRkP5BOTW5R2ekk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:48+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" .
}