@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg> .
@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:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_head {
  this: np:hasAssertion dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_assertion ;
    np:hasProvenance dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_provenance ;
    np:hasPublicationInfo dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_assertion a np:Assertion .
  dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_provenance a np:Provenance .
  dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_assertion {
  miriam-gene:4350 a ncit:C16612 .
  lld:C0001430 a ncit:C7057 .
  dgn-gda:DGN2d6c3df001bc7c294f57f6e4f1467519 sio:SIO_000628 miriam-gene:4350 , lld:C0001430 ;
    a sio:SIO_001121 .
}
dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_provenance {
  dgn-np:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_assertion dcterms:description "[PCR-SSCP and DNA sequence analysis of these induced lesions revealed point mutations at codon 61 of transgenic human c-Has-ras, from CAG (Gln) to CTG (Leu) or CAG (Gln) to AAG (Lyn) in lung hyperplasias (two out of three), an adenoma (one out of two), adenocarcinomas (five out of seven) and forestomach squamous cell carcinomas (four out of five).]. 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:8625461 ;
    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:NP878248.RArk2Zy3SUOUBUshL1bl90MmjKQTHXntEQOzKjdJbfngg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:56+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" .
}