@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw> .
@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:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_head {
  this: np:hasAssertion dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_assertion;
    np:hasProvenance dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_provenance;
    np:hasPublicationInfo dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_assertion a np:Assertion .
  
  dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_provenance a np:Provenance .
  
  dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_assertion {
  miriam-gene:64241 a ncit:C16612 .
  
  lld:C0524620 a ncit:C7057 .
  
  dgn-gda:DGN16f96393aa2c0595278d6ebe84b99a09 sio:SIO_000628 miriam-gene:64241, lld:C0524620;
    a sio:SIO_001121 .
}

dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_provenance {
  dgn-np:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_assertion dcterms:description
      "[Low serum cholesterol and cholesterol absorption were linked to the D19H polymorphism of the ABCG8 gene, and characteristics of the insulin resistance syndrome in men were linked with the Q604E polymorphism of the ABCG5 gene.]. 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:15175352;
    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:NP856030.RAgmWd41O8qcgRG1Iybn6D9M_A88Nuh-4VgGb9XXetMHw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:43+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" .
}