@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k> .
@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:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_head {
  this: np:hasAssertion dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion ;
    np:hasProvenance dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance ;
    np:hasPublicationInfo dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion a np:Assertion .
  dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance a np:Provenance .
  dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion {
  miriam-gene:675 a ncit:C16612 .
  lld:C1336076 a ncit:C7057 .
  dgn-gda:DGNdd83531c2a97e457625f4778e4d2fa8a sio:SIO_000628 miriam-gene:675 , lld:C1336076 ;
    a sio:SIO_001121 .
}
dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_provenance {
  dgn-np:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_assertion dcterms:description "[Certain frequently mutated exons such as 2, 5, 11, 13 and 20 of BRCA1, exons 2, 9, 11 (for 6174delT), 18 and 20 of BRCA2 and 4-9 exons of p53 gene were analyzed in sporadic breast cancer while all 22 coding exons of BRCA1 including its flanking intronic regions along with above mentioned exons of BRCA2 and p53 gene were analyzed in familial breast cancer patients.]. 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:15564800 ;
    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:NP308087.RAla56o82T2w5M6an2iTJptNUUgwW9E36uIX1_oHNEC2k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:57+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" .
}