@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos> .
@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:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_head {
  this: np:hasAssertion dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_assertion;
    np:hasProvenance dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_provenance;
    np:hasPublicationInfo dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_assertion a np:Assertion .
  
  dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_provenance a np:Provenance .
  
  dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_assertion {
  miriam-gene:2348 a ncit:C16612 .
  
  lld:C0678222 a ncit:C7057 .
  
  dgn-gda:DGNc25ecdf6c59289bfca8f6bfe328a52b7 sio:SIO_000628 miriam-gene:2348, lld:C0678222;
    a sio:SIO_001121 .
}

dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_provenance {
  dgn-np:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_assertion dcterms:description
      "[Our findings indicate that Ser1841Asn BRCA1 mutation is able to activate specific protein pathways that are not triggered by other single aminoacid changes and pinpoint to the role TD52 and FOL1 as potential markers in breast cancer patients carrying this particular BRCA1 gene alteration.]. 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:17005433;
    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:NP231830.RA_lyENaRD6ATVLi_GTAqRLFtoY2kdQsZ3eoFUTjtFSos130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:10+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" .
}