@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI> .
@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:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_head {
  this: np:hasAssertion dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_assertion;
    np:hasProvenance dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_provenance;
    np:hasPublicationInfo dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_assertion a np:Assertion .
  
  dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_provenance a np:Provenance .
  
  dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_assertion {
  miriam-gene:6253 a ncit:C16612 .
  
  lld:C0037772 a ncit:C7057 .
  
  dgn-gda:DGN82d06ebc070e8c88a834acb0b1f3c409 sio:SIO_000628 miriam-gene:6253, lld:C0037772;
    a sio:SIO_001121 .
}

dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_provenance {
  dgn-np:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_assertion dcterms:description
      "[In conclusion, these data confirm the presence of SPG10 (chromosome 12), potentially reduce the minimum candidate region for SPG12 (chromosome 19q), and suggest there is at least one additional autosomal dominant SPG locus.]. 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:11354831;
    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:NP237087.RA41xf5DP6z8jzFb4oJcjzhXfjppu1WaBVuv1wBtgD-bI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:13+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" .
}