@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs> .
@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:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_head {
  this: np:hasAssertion dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_assertion ;
    np:hasProvenance dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_provenance ;
    np:hasPublicationInfo dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_assertion a np:Assertion .
  dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_provenance a np:Provenance .
  dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_assertion {
  miriam-gene:1866 a ncit:C16612 .
  lld:C0743332 a ncit:C7057 .
  dgn-gda:DGN5360068329e434e0eb82f755dfae2ae8 sio:SIO_000628 miriam-gene:1866 , lld:C0743332 ;
    a sio:SIO_001121 .
}
dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_provenance {
  dgn-np:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_assertion dcterms:description "[Adult-onset idiopathic focal dystonia affecting specific parts of the body, such as the eye (blepharospasm), neck (cervical dystonia), and hand (writer's cramp), is mostly associated with the DYT7 locus, which was originally mapped to chromosome 18p by genomewide linkage analysis in a large family showing autosomal dominant inheritance.]. 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:16541453 ;
    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:NP449982.RA-FQh1qPFmqcAHWsBJbEM83MilpJUsacmAqjAetR5Lhs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:28+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" .
}