@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE> .
@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:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_head {
  this: np:hasAssertion dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_assertion ;
    np:hasProvenance dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_provenance ;
    np:hasPublicationInfo dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_assertion a np:Assertion .
  dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_provenance a np:Provenance .
  dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  lld:C0022602 a ncit:C7057 .
  dgn-gda:DGN818ed8d6bcbdcd47655f753f1d46269d sio:SIO_000628 miriam-gene:7157 , lld:C0022602 ;
    a sio:SIO_001121 .
}
dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_provenance {
  dgn-np:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_assertion dcterms:description "[Mutations of exons 3 through 9 of the p53 gene in skin lesions were screened in 23 cases of squamous cell carcinoma (SCC), 25 cases of basal cell carcinoma (BCC), two cases of Bowen's disease, 10 cases of solar keratosis, and five cases of keratoacanthoma by polymerase chain reaction--single strand conformation polymorphism analysis.]. 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:8151121 ;
    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:NP197754.RAqamGgZ0Qxhu9HDygSNhlrGhoDBFzFCkSqjiU3g_YJSE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:49+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" .
}