@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ> .
@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:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_head {
  this: np:hasAssertion dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_assertion;
    np:hasProvenance dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_provenance;
    np:hasPublicationInfo dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_assertion a np:Assertion .
  
  dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_provenance a np:Provenance .
  
  dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C1844376 a ncit:C7057 .
  
  dgn-gda:DGNde49029131c99b926b7e9777fb079021 sio:SIO_000628 miriam-gene:1756, lld:C1844376;
    a sio:SIO_001121 .
}

dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_provenance {
  dgn-np:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_assertion dcterms:description
      "[The male fetus and an affected male displayed the same haplotype for RFLPs belonging to six linked loci extending from DXS164 to DXS7, which encompass the CGD locus, and for which the mother was heterozygous.]. 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:2889663;
    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:NP912402.RAiSUgSlhWO-YFVYAPVdCavZNT_GVnHFAFXtWfl-ViYWQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:20+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" .
}