@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U> .
@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:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_head {
  this: np:hasAssertion dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_assertion ;
    np:hasProvenance dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_provenance ;
    np:hasPublicationInfo dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_assertion a np:Assertion .
  dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_provenance a np:Provenance .
  dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_assertion {
  miriam-gene:54498 a ncit:C16612 .
  lld:C3811653 a ncit:C7057 .
  dgn-gda:DGN3416e5c9c3905d0924f3f28f07cb5113 sio:SIO_000628 miriam-gene:54498 , lld:C3811653 ;
    a sio:SIO_001122 .
}
dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_provenance {
  dgn-np:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_assertion dcterms:description "[In addition to those that are potential germline polymorphisms, we found three SMO missense mutations, and one PTCH1 frameshift mutation that are novel and have not been documented in basal cell carcinoma.]. 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:23349881 ;
    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:NP1047112.RAvoPDPmtxJ3xQGdlQRLMHLEkc94Mea3xZA1IJJGnEQ5U130_publicationInfo {
  this: dcterms:created "2016-05-13T12:49:40+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" .
}