@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU> .
@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:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_head {
  this: np:hasAssertion dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_assertion;
    np:hasProvenance dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_provenance;
    np:hasPublicationInfo dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_assertion a np:Assertion .
  
  dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_provenance a np:Provenance .
  
  dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_assertion {
  miriam-gene:3588 a ncit:C16612 .
  
  lld:C0013080 a ncit:C7057 .
  
  dgn-gda:DGN5d260481a362238d09f25949c750339f sio:SIO_000628 miriam-gene:3588, lld:C0013080;
    a sio:SIO_001121 .
}

dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_provenance {
  dgn-np:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_assertion dcterms:description
      "[Given our results, which in some patients were in disagreement with their cytogenetic descriptions, trisomy for locus D21S13 through locus D21S58 is excluded from significant contribution to many Down syndrome features.]. 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:2529205;
    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:NP213881.RA6hl7OZtc_RgCDKjob2P2lldi4kLEjUfzu06qdGad5MU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}