@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc> .
@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:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_head {
  this: np:hasAssertion dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion ;
    np:hasProvenance dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance ;
    np:hasPublicationInfo dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion a np:Assertion .
  dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance a np:Provenance .
  dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion {
  miriam-gene:2811 a ncit:C16612 .
  lld:C0005129 a ncit:C7057 .
  dgn-gda:DGN813b24ba5072c323b78e4aad00c15ce7 sio:SIO_000628 miriam-gene:2811 , lld:C0005129 ;
    a sio:SIO_001121 .
}
dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_provenance {
  dgn-np:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_assertion dcterms:description "[Underlying this disorder of platelet function is a defect in the platelet glycoprotein (GP) Ib-IX-V complex, composed of four polypeptides, GP Ib alpha, GP Ib beta, GP IX, and GP V. Molecular characterization of individuals with BSs has identified mutations in the GP Ib alpha, GP Ib beta, and GP IX genes responsible for the expressed phenotype.]. 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:10996832 ;
    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:NP375658.RA998marqstufhMw97urongvyeW7q7k0SHpHEzRzWIVRc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:40+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" .
}