@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo
> .
@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:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_head
{
this:
np:hasAssertion
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_assertion
;
np:hasProvenance
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_assertion
a
np:Assertion
.
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_provenance
a
np:Provenance
.
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_assertion
{
miriam-gene:4838
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN88b8b7977cdf48c7884c229d8d2b359d
sio:SIO_000628
miriam-gene:4838
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_provenance
{
dgn-np:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_assertion
dcterms:description
"[We confirmed the contribution to CHD of copy number changes in genes such as GATA4 and NODAL and identified several genes in novel recurrent CNVs that may point to novel CHD candidate loci.]. 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:23979609
;
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:NP1105590.RAGq_-s0LjRBE9PgTCwkECE94WmvN_sfvDT0EyfVLpjLo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:07+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" .
}