@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8> .
@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:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_head {
  this: np:hasAssertion dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_assertion;
    np:hasProvenance dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_provenance;
    np:hasPublicationInfo dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_assertion a np:Assertion .
  
  dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_provenance a np:Provenance .
  
  dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_assertion {
  miriam-gene:11001 a ncit:C16612 .
  
  lld:C1527231 a ncit:C7057 .
  
  dgn-gda:DGN433b7cae0dc98ee0b8c6be1d7bcbb632 sio:SIO_000628 miriam-gene:11001, lld:C1527231;
    a sio:SIO_001121 .
}

dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_provenance {
  dgn-np:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_assertion dcterms:description
      "[To elucidate the mechanisms underlying the phenotypic variability of ALD, we studied the expression of ABCD1, three other peroxisomal transporter genes of the same family (ABCD2, ABCD3 and ABCD4) and two VLCFA synthetase genes (VLCS and BG1) involved in VLCFA metabolism, as well as the VLCFA concentrations in the normal white matter (WM) from ALD patients with CCER, AMN-C and AMN phenotypes.]. 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:15800013;
    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:NP632442.RAi8ts6S2makF9M1U2J0vS2hsh4usXJPtpX2vmU_Scti8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:21+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" .
}