@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws> .
@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:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_head {
  this: np:hasAssertion dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_assertion;
    np:hasProvenance dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_provenance;
    np:hasPublicationInfo dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_assertion a np:Assertion .
  
  dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_provenance a np:Provenance .
  
  dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_assertion {
  miriam-gene:5460 a ncit:C16612 .
  
  lld:C0033860 a ncit:C7057 .
  
  dgn-gda:DGN696453974e910ae9a7714b618a0d357f sio:SIO_000628 miriam-gene:5460, lld:C0033860;
    a sio:SIO_001121 .
}

dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_provenance {
  dgn-np:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_assertion dcterms:description
      "[Combinatorial analysis of exonic variations in the known genes of the candidate interval revealed that HCG27, PSORS1C3, OTF3, TCF19, HCR, STG, and HCG22 bore no alleles unique to risk haplotypes among the 10 sequenced haplotypes.]. 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:16642438;
    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:NP905061.RAR0CDbQBlWnnxnl1HPaDoWB5CqU3t3pq6zODEa_myGws130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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: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" .
}