@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM> .
@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:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_head {
  this: np:hasAssertion dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion;
    np:hasProvenance dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance;
    np:hasPublicationInfo dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion a np:Assertion .
  
  dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance a np:Provenance .
  
  dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion {
  miriam-gene:57679 a ncit:C16612 .
  
  lld:C0234131 a ncit:C7057 .
  
  dgn-gda:DGN0904c62c077af9ccc4263fdfb2ee35a8 sio:SIO_000628 miriam-gene:57679, lld:C0234131;
    a sio:SIO_001121 .
}

dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance {
  dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion dcterms:description
      "[These mouse models largely fail to recapitulate hallmarks of motor neuron disease, but the subtle deficits that are observed in behavior and pathology have aided in our understanding of the relationship between alsin and motor dysfunction.]. 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:17955197;
    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:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:47+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" .
}