@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y
> .
@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:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_head
{
this:
np:hasAssertion
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_assertion
;
np:hasProvenance
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_assertion
a
np:Assertion
.
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_provenance
a
np:Provenance
.
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_assertion
{
miriam-gene:23493
a
ncit:C16612
.
lld:C0018818
a
ncit:C7057
.
dgn-gda:DGNf87720d9433d32bfb6dc920df0ecc3c7
sio:SIO_000628
miriam-gene:23493
,
lld:C0018818
;
a
sio:SIO_001121
.
}
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_provenance
{
dgn-np:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_assertion
dcterms:description
"[By direct sequencing, we analyzed the sequences encoding the bHLH domain of the human HEY2 in 52 explanted hearts of unrelated patients with complex cardiac malformations, notably ventricular (VSD) and atrioventricular septal defects (AVSD).]. 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:16329098
;
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:NP708866.RAOQkLnl_6YOJ5CsdI-SqE3OetV56x_33t77lNgUiG89Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}