@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE> .
@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:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_head {
  this: np:hasAssertion dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_assertion;
    np:hasProvenance dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_provenance;
    np:hasPublicationInfo dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_assertion a np:Assertion .
  
  dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_provenance a np:Provenance .
  
  dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_assertion {
  miriam-gene:1761 a ncit:C16612 .
  
  lld:C0002871 a ncit:C7057 .
  
  dgn-gda:DGN05ea921c6b2b490cc55fcc7f1687f46a sio:SIO_000628 miriam-gene:1761, lld:C0002871;
    a sio:SIO_001121 .
}

dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_provenance {
  dgn-np:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_assertion dcterms:description
      "[Our data confirm the major role of DMT1 in the maintenance of iron homeostasis in humans and demonstrate that the N491S mutation, through its deleterious effect on protein trafficking, contributes together with the G212V mutation to the development of anemia and hepatic iron overload.]. 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:21871825;
    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:NP575170.RACR0Hea8MyDL0ZnSFrLcy49D6a4-8508T6OeRPRmXafE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:47+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" .
}