@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw> .
@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:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_head {
  this: np:hasAssertion dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_assertion;
    np:hasProvenance dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_provenance;
    np:hasPublicationInfo dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_assertion a np:Assertion .
  
  dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_provenance a np:Provenance .
  
  dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_assertion {
  miriam-gene:538 a ncit:C16612 .
  
  lld:C0268070 a ncit:C7057 .
  
  dgn-gda:DGN40c2b2e2d82ed0b774fac4e35ee8318f sio:SIO_000628 miriam-gene:538, lld:C0268070;
    a sio:SIO_001121 .
}

dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_provenance {
  dgn-np:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_assertion dcterms:description
      "[Adequate supplies of copper are particularly important in developing animals, and in humans this is illustrated by mutations of ATP7A that cause the copper deficiency condition Menkes disease, which is fatal in early childhood.]. 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:12730448;
    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:NP457405.RAl_e2iNUnL0pS6V6raIL1UUPQHg3p6QwhwWLQSSrKRsw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:32+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" .
}