@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48> .
@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:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_head {
  this: np:hasAssertion dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_assertion;
    np:hasProvenance dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_provenance;
    np:hasPublicationInfo dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_assertion a np:Assertion .
  
  dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_provenance a np:Provenance .
  
  dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_assertion {
  miriam-gene:6638 a ncit:C16612 .
  
  lld:C0151786 a ncit:C7057 .
  
  dgn-gda:DGN5cbc405f86650f4fd30eff0ed815e05a sio:SIO_000628 miriam-gene:6638, lld:C0151786;
    a sio:SIO_001121 .
}

dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_provenance {
  dgn-np:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_assertion dcterms:description
      "[This genetic alteration results in reduced levels of the SMN protein, leading to degeneration of alpha motor neurons of the spinal cord and resulting in muscle weakness and progressive symmetrical proximal paralysis.]. 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:20711542;
    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:NP323985.RATyciHmGaf0zaiZTgqF5t0kr28LkoO7XEiWl8UwUOZ48130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:09+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" .
}