@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg> .
@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/v4.0.0/void/> .

dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_head {
  this: np:hasAssertion dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_assertion;
    np:hasProvenance dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_provenance;
    np:hasPublicationInfo dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_assertion a np:Assertion .
  
  dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_provenance a np:Provenance .
  
  dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_assertion {
  miriam-gene:5573 a ncit:C16612 .
  
  lld:C0750929 a ncit:C7057 .
  
  dgn-gda:DGNa2ac0217e2812135eb3f63cb945e264a sio:SIO_000628 miriam-gene:5573, lld:C0750929;
    a sio:SIO_001121 .
}

dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_provenance {
  dgn-np:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_assertion dcterms:description
      "[Several identified eQTLs were novel and these implicate genes involved in bone development (IPO8, XYLT1, and PRKAR1A), and ribosomal pathways related to marrow and bone dysfunction, as potential candidates in the development of CMI.]. 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:25609184;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1257399.RA0C0VtdYb0uZ0TnGfP3rr-ZTgOFZIO6ZKCmnZLuB9Leg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:16+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}