@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE> .
@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:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_head {
  this: np:hasAssertion dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_assertion ;
    np:hasProvenance dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_provenance ;
    np:hasPublicationInfo dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_assertion a np:Assertion .
  dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_provenance a np:Provenance .
  dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_assertion {
  miriam-gene:2810 a ncit:C16612 .
  lld:C0442874 a ncit:C7057 .
  dgn-gda:DGN417be3e8388d4a1da17e4c8e61edbe5f sio:SIO_000628 miriam-gene:2810 , lld:C0442874 ;
    a sio:SIO_001121 .
}
dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_provenance {
  dgn-np:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_assertion dcterms:description "[Patients referred with possible I-SFN, who met the criteria of ≥2 SFN-related symptoms, normal strength, tendon reflexes, vibration sense, and nerve conduction studies, and reduced intraepidermal nerve fiber density (IENFD) plus abnormal quantitative sensory testing (QST) and no underlying etiology for SFN, were assessed clinically and by screening of SCN9A for mutations and functional analyses.]. 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:21698661 ;
    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:NP656082.RA6GPbb-6dE9DmOurckHIUSuhi_5nP-Dr410fH-sde5cE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:35+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" .
}