@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI> .
@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:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_head {
  this: np:hasAssertion dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_assertion ;
    np:hasProvenance dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_provenance ;
    np:hasPublicationInfo dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_assertion a np:Assertion .
  dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_provenance a np:Provenance .
  dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_assertion {
  miriam-gene:5726 a ncit:C16612 .
  lld:C0596263 a ncit:C7057 .
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    a sio:SIO_001121 .
}
dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_provenance {
  dgn-np:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_assertion dcterms:description "[To investigate the possible role of the PTC gene on chromosome 9q22.3, that was identified as the cause of nevoid basal cell carcinoma syndrome, during carcinogenesis in esophagus and lung, we examined 20 esophageal squamous cell carcinomas and 10 squamous cell carcinomas of the lung for mutations in any coding exon of PTC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP488068.RAopDLFhwnlGqoFzjcmXS0zhcO_Jbr2if_ZydKp-FuFlI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:51+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 ;
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}