@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk> .
@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:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_head {
  this: np:hasAssertion dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion;
    np:hasProvenance dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance;
    np:hasPublicationInfo dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion a np:Assertion .
  
  dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance a np:Provenance .
  
  dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion {
  miriam-gene:6683 a ncit:C16612 .
  
  lld:C0443306 a ncit:C7057 .
  
  dgn-gda:DGNfe2c4e88b401efe33db5004ebbe1bf06 sio:SIO_000628 miriam-gene:6683, lld:C0443306;
    a sio:SIO_001121 .
}

dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_provenance {
  dgn-np:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_assertion dcterms:description
      "[The most common forms of hereditary spastic paraplaegia are SPG4 and SPG3A caused by sequence variants in the SPAST and ATL1 genes, as well as by deletions and duplications not detected by standard techniques.]. 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:22203332;
    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:NP266207.RAfkNX9UnwLxjFcmtUa_1rhvkmgbJEs39-mUVu1fWoFkk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}