@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo> .
@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:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_head {
  this: np:hasAssertion dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_assertion;
    np:hasProvenance dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_provenance;
    np:hasPublicationInfo dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_assertion a np:Assertion .
  
  dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_provenance a np:Provenance .
  
  dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_assertion {
  miriam-gene:6606 a ncit:C16612 .
  
  lld:C0085084 a ncit:C7057 .
  
  dgn-gda:DGNec4f87177c7c3aed9f6c8c13937fdfb0 sio:SIO_000628 miriam-gene:6606, lld:C0085084;
    a sio:SIO_001122 .
}

dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_provenance {
  dgn-np:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_assertion dcterms:description
      "[The association between survivor motor neuron (SMN) gene deletions and motor neuron diseases such as spinal muscular atrophy (SMA) and amyotrophic lateral sclerosis (ALS) suggest that sporadic lower motor neuron disease (LMND) may be related to SMN gene deletion.]. 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:20947812;
    prov:wasDerivedFrom dgn-void:gad-20130706;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP92189.RArkBnJkVDXxQWJr6kwZdL_1hCmEI0xhcGIYo7OKLqYoo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+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" .
}