@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw> .
@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 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:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_head {
  this: np:hasAssertion dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_assertion;
    np:hasProvenance dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_provenance;
    np:hasPublicationInfo dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_assertion a np:Assertion .
  
  dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_provenance a np:Provenance .
  
  dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_assertion {
  miriam-gene:345 a ncit:C16612 .
  
  lld:C0020473 a ncit:C7057 .
  
  dgn-gda:DGNb387c59041178793865ce66d6bf6f1a7 sio:SIO_000628 miriam-gene:345, lld:C0020473;
    a sio:SIO_001122 .
}

dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_provenance {
  dgn-np:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_assertion dct:description
      "[While these effects can be attributed to the presence of the M2 and S2 minor alleles, these results suggest that the importance of specific allelic haplotypes may be greater than single genotypic effects.]. 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:11181747;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP59581.RA4YqHoOXYV4T1FJ9E2jCCubqjzIuyZL1EsIOcR-fuEvw130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}