@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_head {
  this: np:hasAssertion dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_assertion ;
    np:hasProvenance dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_provenance ;
    np:hasPublicationInfo dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_provenance a np:Provenance .
  dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_assertion {
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dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_provenance {
  dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_assertion dcterms:description "[These genes are important in bone morphology, metabolism and vascular disease. Our results may provide insight into the pathogenesis of osteonecrosis in sickle cell disease, help identify individuals who are at high risk for osteonecrosis, and thus allow ]. 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:15784727 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
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  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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}
dgn-np:NP76508.RAJ7M34-HBD0xWLFHXxhIQAgEjAt36qvnBj2q1BrykSbE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:22+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
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}