@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40> .
@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:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_head {
  this: np:hasAssertion dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_assertion ;
    np:hasProvenance dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_provenance ;
    np:hasPublicationInfo dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_assertion a np:Assertion .
  dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_provenance a np:Provenance .
  dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_assertion {
  miriam-gene:137814 a ncit:C16612 .
  lld:C0010068 a ncit:C7057 .
  dgn-gda:DGN4d5db76ca33dff618ea7097136bb6155 sio:SIO_000628 miriam-gene:137814 , lld:C0010068 ;
    a sio:SIO_001121 .
}
dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_provenance {
  dgn-np:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_assertion dcterms:description "[This study firstly links NKX2.6 loss-of-function mutation with increased susceptibility to isolated VSD, providing novel insight into the molecular mechanism underpinning VSD and contributing to the development of new preventive and therapeutic strategies for this common form of CHD.]. 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:25380965 ;
    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:NP1235979.RAnnPBn1JY93PGo1yxI0aCV2EpSJ2zknwQcCcLAySBU40130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:06+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" .
}