@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0> .
@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:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_head {
  this: np:hasAssertion dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion;
    np:hasProvenance dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance;
    np:hasPublicationInfo dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion a np:Assertion .
  
  dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance a np:Provenance .
  
  dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion {
  miriam-gene:64132 a ncit:C16612 .
  
  lld:C0268654 a ncit:C7057 .
  
  dgn-gda:DGNcfd37ae69fce89fe5527cca0bba8f974 sio:SIO_000628 miriam-gene:64132, lld:C0268654;
    a sio:SIO_001121 .
}

dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_provenance {
  dgn-np:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_assertion dcterms:description
      "[Additional mutations were identified in the genes encoding the putative glycine transporter SLC6A18 (XT2) and the neutral amino acid transporter SLC6A19 (B0AT1) in families with either IG or HG, suggesting that mutations in the genes encoding these transporters may also contribute to these phenotypes.]. 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:19033659;
    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:NP161105.RATLP9DJ8xhKUah0GmifupOzG_N0WIaFnFd388lsj61C0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:27+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" .
}