@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ> .
@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/v4.0.0/void/> .

dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_head {
  this: np:hasAssertion dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion;
    np:hasProvenance dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_provenance;
    np:hasPublicationInfo dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion a np:Assertion .
  
  dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_provenance a np:Provenance .
  
  dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion {
  miriam-gene:1827 a ncit:C16612 .
  
  lld:C0025362 a ncit:C7057 .
  
  dgn-gda:DGNbc0995dda2256781ae83224445f8782d sio:SIO_000628 miriam-gene:1827, lld:C0025362;
    a sio:SIO_001121 .
}

dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_provenance {
  dgn-np:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_assertion dcterms:description
      "[These results, combined with our data showing that the same biochemical signaling pathway is altered in human DS fetal brain tissue overexpressing DSCR1, suggest that alteration of DSCR1 expression could contribute to mental retardation in DS.]. 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:14668437;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP423938.RAMs4h_ce7wOvilHETQzxg15EYNfH7lM9em-KQW2_TQUQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:57+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}