@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_head {
  this: np:hasAssertion dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_assertion;
    np:hasProvenance dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_provenance;
    np:hasPublicationInfo dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_assertion a np:Assertion .
  
  dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_provenance a np:Provenance .
  
  dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_assertion {
  miriam-gene:3508 a ncit:C16612 .
  
  lld:C0026847 a ncit:C7057 .
  
  dgn-gda:DGN3e9e0d587701dfce90a9d12735fa527b sio:SIO_000628 miriam-gene:3508, lld:C0026847;
    a sio:SIO_001121 .
}

dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_provenance {
  dgn-np:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_assertion dcterms:description
      "[Our results show that IGHMBP2 is the second gene found to be defective in spinal muscular atrophy, and indicate that IGHMBP2 and SMN share common functions important for motor neuron maintenance and integrity in mammals.]. 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:11528396;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP486888.RAnim8FNg9FNI1f9rMGivTsPrK_Mn-6g5vFM6m2MshDtg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:42:27+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}