@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus> .
@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:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_head {
  this: np:hasAssertion dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_assertion;
    np:hasProvenance dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_provenance;
    np:hasPublicationInfo dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_assertion a np:Assertion .
  
  dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_provenance a np:Provenance .
  
  dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_assertion {
  miriam-gene:3925 a ncit:C16612 .
  
  lld:C0085084 a ncit:C7057 .
  
  dgn-gda:DGNae79d01b883e001906614b90b21431f3 sio:SIO_000628 miriam-gene:3925, lld:C0085084;
    a sio:SIO_001121 .
}

dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_provenance {
  dgn-np:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_assertion dcterms:description
      "[These findings demonstrate that other components of the SMN complex, in addition to SMN, are critical for the activity of the complex and suggest that Gemin2 and Gemin6 are potentially important modifiers of SMA as well as potential disease genes for non-SMN motor neuron diseases.]. 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:15843395;
    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:NP495353.RATojkCwIyvqvLOOFRSpYeXZVgfSiK5du4r8Wpy1-vPus130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:55+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" .
}