@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4> .
@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:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_head {
  this: np:hasAssertion dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion;
    np:hasProvenance dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance;
    np:hasPublicationInfo dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion a np:Assertion .
  
  dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance a np:Provenance .
  
  dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion {
  miriam-gene:1861 a ncit:C16612 .
  
  lld:C0338902 a ncit:C7057 .
  
  dgn-gda:DGN7e405b514e398bc0d837c5294951ecc9 sio:SIO_000628 miriam-gene:1861, lld:C0338902;
    a sio:SIO_001121 .
}

dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_provenance {
  dgn-np:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_assertion dcterms:description
      "[Genetic haplotypes at five marker loci that are closely linked to the DYT1 gene on chromosome 9q were determined in 10 Ashkenazi Jewish patients with focal hand dystonia (eight with musician's cramp, two with writer's cramp).]. 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:8684386;
    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:NP858144.RAu1S74FSO-Qc6_VLjlhoZQ9H1yj3wt08zws4TX2p-ca4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:44+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" .
}