@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08> .
@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:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_head {
  this: np:hasAssertion dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_assertion ;
    np:hasProvenance dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_provenance ;
    np:hasPublicationInfo dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_assertion a np:Assertion .
  dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_provenance a np:Provenance .
  dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_assertion {
  miriam-gene:5660 a ncit:C16612 .
  lld:C0005779 a ncit:C7057 .
  dgn-gda:DGN62e3bceee4388be738c41e2c8fc4e2bb sio:SIO_000628 miriam-gene:5660 , lld:C0005779 ;
    a sio:SIO_001121 .
}
dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_provenance {
  dgn-np:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_assertion dcterms:description "[None of the 21 patients had hereditary deficiencies of antithrombin III, protein C, or protein S. Our results indicate that the milder bleeding diathesis that is occasionally seen among Italian hemophiliacs with factor levels that are less than 1 percent cannot be explained by the concomitant expression of a known prothrombotic defect.]. 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:8607105 ;
    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:NP691274.RApgvvXostZNXyf9QXRcg6uz-XyGWS8vrGFgvKnZGwC08130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:00+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" .
}