@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc> .
@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:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_head {
  this: np:hasAssertion dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_assertion ;
    np:hasProvenance dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_provenance ;
    np:hasPublicationInfo dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_assertion a np:Assertion .
  dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_provenance a np:Provenance .
  dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_assertion {
  miriam-gene:2908 a ncit:C16612 .
  lld:C0029458 a ncit:C7057 .
  dgn-gda:DGN57df4260c7e2333842012828e0bb8211 sio:SIO_000628 miriam-gene:2908 , lld:C0029458 ;
    a sio:SIO_001122 .
}
dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_provenance {
  dgn-np:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_assertion dcterms:description "[When compared to currently used PCR-based restriction fragment length polymorphism (RFLP) and direct DNA sequencing methods, the new allele-specific PCR method showed 100% accuracy for the detection of Asn363Asn and Asn363Ser genotypes. The feasibility of these methods were tested in 301 patients, including 47 patients with postmenopausal osteoporosis in whom the frequency of Asn363Ser polymorphism was similar to that found in control subjects (4.3% versus 4.4%).]. 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:15698551 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP53627.RAYYzIpTs5THSagSzvfqLS2xZBzuEm1hZriTd-gsNC-Fc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:25+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" .
}