@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68> .
@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/v4.0.0/void/> .

dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_head {
  this: np:hasAssertion dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_assertion;
    np:hasProvenance dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_provenance;
    np:hasPublicationInfo dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_assertion a np:Assertion .
  
  dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_provenance a np:Provenance .
  
  dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_assertion {
  miriam-gene:11146 a ncit:C16612 .
  
  lld:C0751658 a ncit:C7057 .
  
  dgn-gda:DGNb783c6d295abe1abc9d6b242346758b1 sio:SIO_000628 miriam-gene:11146, lld:C0751658;
    a sio:SIO_001122 .
}

dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_provenance {
  dgn-np:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_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-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP753055.RAKx4lr1LpDeWOxUeBslowliEVMncedjlQdm4Zu3skl68130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:26+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}