@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI> .
@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:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_head {
  this: np:hasAssertion dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_assertion;
    np:hasProvenance dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_provenance;
    np:hasPublicationInfo dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_assertion a np:Assertion .
  
  dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_provenance a np:Provenance .
  
  dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_assertion {
  miriam-gene:1081 a ncit:C16612 .
  
  lld:C0007133 a ncit:C7057 .
  
  dgn-gda:DGN8c4712c3457c2eb76aacbf1301338a01 sio:SIO_000628 miriam-gene:1081, lld:C0007133;
    a sio:SIO_001121 .
}

dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_provenance {
  dgn-np:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_assertion dcterms:description
      "[Two of five PDC cases and one papillary carcinoma revealed point mutations in exon 8 as follows; GTG (val) to CTG (leu) at codon 272 in case 23T, CGA (arg) to CCA (pro) at codon 306 in case of 30T, and CGG (arg) to AGG (arg) at codon 282 in case 28T.]. 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:8616809;
    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:NP746930.RACbkGRfF6yTLLF2YFubFTd_ndtfRCKt2A1O10lLR_cEI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:33+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" .
}