@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts> .
@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:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_head {
  this: np:hasAssertion dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_assertion;
    np:hasProvenance dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_provenance;
    np:hasPublicationInfo dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_assertion a np:Assertion .
  
  dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_provenance a np:Provenance .
  
  dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_assertion {
  miriam-gene:1056 a ncit:C16612 .
  
  lld:C0751658 a ncit:C7057 .
  
  dgn-gda:DGN6f57b7da7ef718704ce16e5cb8dac1f1 sio:SIO_000628 miriam-gene:1056, lld:C0751658;
    a sio:SIO_001121 .
}

dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_provenance {
  dgn-np:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_assertion dcterms:description
      "[Although concomitant lesions in the ulnar nerve entrapment site at the wrist cannot be excluded, these findings indicate that CTS is not the sole distinctive feature in the majority of FAP ATTR Val30Met patients.]. 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:19626479;
    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:NP728250.RAGhDhH4nGNT1nYDB9ibl-gaEVGf-zCdnh_4aVS_jUbts130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:22+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" .
}