@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw> .
@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:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_head {
  this: np:hasAssertion dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_assertion;
    np:hasProvenance dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_provenance;
    np:hasPublicationInfo dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_assertion a np:Assertion .
  
  dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_provenance a np:Provenance .
  
  dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_assertion {
  miriam-gene:4485 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN75e3ed86e7f079e4364d36cbd9c720c6 sio:SIO_000628 miriam-gene:4485, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_provenance {
  dgn-np:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_assertion dcterms:description
      "[Genetic defects in MSP implicate a range of biological mechanisms including RNA processing and protein homeostasis, both with potential relevance to the pathobiology of more common MNDs such as amyotrophic lateral sclerosis (ALS) and providing an additional link between ALS and FTD.]. 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:23635965;
    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:NP251761.RAeSfxAmCK3_5Z2UCNn3OZIibnvAvFavS25tcEXf4mLPw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:20+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" .
}