@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA> .
@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:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_head {
  this: np:hasAssertion dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_assertion;
    np:hasProvenance dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_provenance;
    np:hasPublicationInfo dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_assertion a np:Assertion .
  
  dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_provenance a np:Provenance .
  
  dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_assertion {
  miriam-gene:9780 a ncit:C16612 .
  
  lld:C0011175 a ncit:C7057 .
  
  dgn-gda:DGN052672e628a03de0d5e294aa4d96330f sio:SIO_000628 miriam-gene:9780, lld:C0011175;
    a sio:SIO_001121 .
}

dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_provenance {
  dgn-np:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_assertion dcterms:description
      "[Familial xerocytosis (HX) in humans is an autosomal disease that causes dehydration of red blood cells resulting in hemolytic anemia which has been traced to two individual mutations in the mechanosensitive ion channel, PIEZO1.]. 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:23487776;
    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:NP713276.RATGMTroFYhmtt0RWxIbvHgruCYM96T7Vbx4qCZOL2iLA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:13+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" .
}