@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA> .
@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:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_head {
  this: np:hasAssertion dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_assertion;
    np:hasProvenance dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_provenance;
    np:hasPublicationInfo dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_assertion a np:Assertion .
  
  dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_provenance a np:Provenance .
  
  dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_assertion {
  miriam-gene:6607 a ncit:C16612 .
  
  lld:C0151514 a ncit:C7057 .
  
  dgn-gda:DGN4a5a07cae05dac2cd35efb807cd2a5ad sio:SIO_000628 miriam-gene:6607, lld:C0151514;
    a sio:SIO_001121 .
}

dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_provenance {
  dgn-np:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_assertion dcterms:description
      "[Notably, SMN deficiency in SMA leads to the aberrant subcellular localization of Gemin8 and PP1γ in the atrophic skeletal muscles, suggesting that the function of PP1γ is likely to be affected in disease.]. 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:22454514;
    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:NP708025.RAe_aPpuO_GYehAV25G5LEBLiNiC0OEakW1uGMkIv9LIA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:10+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" .
}