@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs> .
@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:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_head {
  this: np:hasAssertion dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_assertion ;
    np:hasProvenance dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_provenance ;
    np:hasPublicationInfo dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_assertion a np:Assertion .
  dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_provenance a np:Provenance .
  dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_assertion {
  miriam-gene:2778 a ncit:C16612 .
  lld:C1864100 a ncit:C7057 .
  dgn-gda:DGN7a9363a2bd0d58ced718cae82c28fe00 sio:SIO_000628 miriam-gene:2778 , lld:C1864100 ;
    a sio:SIO_001121 .
}
dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_provenance {
  dgn-np:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_assertion dcterms:description "[Besides representing a murine autosomal-dominant pseudohypoparathyroidism type Ib model and one of only few animal models for imprinted human disorders, our findings suggest that the Nesp55 differentially methylated region is an additional principal imprinting control region, which directs Gnas methylation and thereby affects expression of all maternal Gnas-derived transcripts.]. 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:20427744 ;
    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:NP374081.RAXJzO7ho9R9LrcItWbSPoSWxNFc7y3rMxrz-UpKISJNs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:39+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" .
}