@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_head {
   this: np:hasAssertion dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_assertion ;
    np:hasProvenance dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_provenance ;
    np:hasPublicationInfo dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_assertion a np:Assertion .
  dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_provenance a np:Provenance .
  dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_assertion {
   miriam-gene:7276 a ncit:C16612 .
  lld:C0751658 a ncit:C7057 .
  dgn-gda:DGN43a67aa1ccf2cb008ecf46a2167e3a41 sio:SIO_000628 miriam-gene:7276 , lld:C0751658 ;
    a sio:SIO_001122 .
}
dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_provenance {
   dgn-np:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_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-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP761938.RAVgp-MxWNDoDRQcZVW6PfwBELxNx7EqqbiX66mi4q8OA130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:20+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}