@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc
> .
@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:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_head
{
this:
np:hasAssertion
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_assertion
;
np:hasProvenance
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_provenance
;
np:hasPublicationInfo
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_assertion
a
np:Assertion
.
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_provenance
a
np:Provenance
.
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_assertion
{
miriam-gene:5350
a
ncit:C16612
.
lld:C0039685
a
ncit:C7057
.
dgn-gda:DGN92b523551ab6ea25974d8a6ca5968c4e
sio:SIO_000628
miriam-gene:5350
,
lld:C0039685
;
a
sio:SIO_001121
.
}
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_provenance
{
dgn-np:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_assertion
dcterms:description
"[Our objective was to evaluate SERCA2a (i.e., the SERCA cardiac isoform), PLN, SLN, and RyR2 (i.e., the RyR isoform enriched in the heart) gene expression in myocardial tissue of patients affected by tetralogy of Fallot (TOF), a conotruncal heart defect.]. 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:17515962
;
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:NP896124.RAcswwEVlVt_M7RO1tAjUeohMTXUlTM1_04SMXdLDTjqc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}