@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8> .
@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 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:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_head {
  this: np:hasAssertion dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_assertion;
    np:hasProvenance dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_provenance;
    np:hasPublicationInfo dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_assertion a np:Assertion .
  
  dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_provenance a np:Provenance .
  
  dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_assertion {
  miriam-gene:8487 a ncit:C16612 .
  
  lld:C0026847 a ncit:C7057 .
  
  dgn-gda:DGN6998d446b3318b8d6f6d2ba36ab22517 sio:SIO_000628 miriam-gene:8487, lld:C0026847;
    a sio:SIO_001121 .
}

dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_provenance {
  dgn-np:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_assertion dc:description
      "[These findings suggest that an aberrant alternative splicing event in SIP1 occurs tissues derived from patients with the motor neuron diseases, and contributes to the pathological process of SMA and ALS.]. 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:11943600;
    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:NP380886.RABZ6y_dxahnVKGGMoG72hbhpMCaOjsigy_8i8HcwIHc8130_publicationInfo {
  this: dc:created "2014-10-02T12:35:45+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}