@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU> .
@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/v3.0.0/void/> .

dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_head {
  this: np:hasAssertion dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion;
    np:hasProvenance dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance;
    np:hasPublicationInfo dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion a np:Assertion .
  
  dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance a np:Provenance .
  
  dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion {
  miriam-gene:26154 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGN3229e9147bdef2c0bde186068264bdb7 sio:SIO_000628 miriam-gene:26154, lld:C0019247;
    a sio:SIO_001121 .
}

dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_provenance {
  dgn-np:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_assertion dcterms:description
      "[This article describes ABCA12 as a causative molecule involved in defects in HI, summarizes the known genetic disorders caused by genetic defects in ABCA lipid transporters, and highlights the prospects of prenatal diagnosis and gene therapy for HI.]. 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:16847209;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP882061.RANy9RDZoc2WE0FtQjtn8tBq5Ts15gtLf3msZ2hAxQSCU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:37+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}