@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE> .
@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:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_head {
  this: np:hasAssertion dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion;
    np:hasProvenance dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance;
    np:hasPublicationInfo dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion a np:Assertion .
  
  dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance a np:Provenance .
  
  dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion {
  miriam-gene:7190 a ncit:C16612 .
  
  lld:C0037772 a ncit:C7057 .
  
  dgn-gda:DGNeb0e5d19d2ae123185692574c17ed54c sio:SIO_000628 miriam-gene:7190, lld:C0037772;
    a sio:SIO_001121 .
}

dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_provenance {
  dgn-np:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_assertion dcterms:description
      "[HSP is classified according to the mode of inheritance, the HSP locus when known, and whether the spastic paraplegia syndrome occurs alone or is accompanied by additional neurologic or systemic abnormalities.]. 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:16469273;
    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:NP423705.RA9dN6MZmLmR4ZoUqlsgCYfUDtzfvZ_9-IQKPFh3LreNE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:11+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" .
}