@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w> .
@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:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_head {
  this: np:hasAssertion dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion;
    np:hasProvenance dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance;
    np:hasPublicationInfo dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion a np:Assertion .
  
  dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance a np:Provenance .
  
  dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion {
  miriam-gene:7299 a ncit:C16612 .
  
  lld:C0019880 a ncit:C7057 .
  
  dgn-gda:DGN537a0e40496fbfcac26e124f7e54e398 sio:SIO_000628 miriam-gene:7299, lld:C0019880;
    a sio:SIO_001121 .
}

dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_provenance {
  dgn-np:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_assertion dcterms:description
      "[Our data suggest that reversible hypopigmentation in homocystinuria is the result of tyrosinase inhibition by homocyst(e)ine and that the probable mechanism of this inhibition is the interaction of homocyst(e)ine with copper at the active site of tyrosinase.]. 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:7611281;
    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:NP772607.RAcd1lDdVDXqrbASm8aNHhPloy0FsdXPpcqzLWBlsmX3w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:47+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" .
}