@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI> .
@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:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_head {
  this: np:hasAssertion dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_assertion;
    np:hasProvenance dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_provenance;
    np:hasPublicationInfo dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_assertion a np:Assertion .
  
  dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_provenance a np:Provenance .
  
  dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_assertion {
  miriam-gene:7306 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN5780ec9bdf89cf7a6c89c7ad7bcdacdd sio:SIO_000628 miriam-gene:7306, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_provenance {
  dgn-np:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_assertion dcterms:description
      "[The list of confirmed 'channelopathies' is growing and several members of the TRP family of ion channels have been implicated in human diseases such as mucolipidosis type IV (MLIV), autosomal dominant polycystic kidney disease (ADPKD), familial focal segmental glomerulosclerosis (FSG), hypomagnesemia with secondary hypocalcaemia (HSH), and several forms of cancer.]. 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:17138610;
    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:NP260625.RAmJP0t7KH8kIvIU0MEZB3mreMCFATG1IJb3ivpMT7qTI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:25+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" .
}