@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8
> .
@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:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_head
{
this:
np:hasAssertion
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion
a
np:Assertion
.
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_provenance
a
np:Provenance
.
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_assertion
{
miriam-gene:2626
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN58d6facee00d776ddeeb0e95c6d471f3
sio:SIO_000628
miriam-gene:2626
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_provenance
{
dgn-np:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_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:NP1105591.RAmhdmPPAgjVqowW5tPa71ySBKczWdug2MXPKz0hdZqu8130_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
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;
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" .
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pav:version
"v4.0.0" .
}