@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4
> .
@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:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_head
{
this:
np:hasAssertion
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_assertion
;
np:hasProvenance
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_assertion
a
np:Assertion
.
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_provenance
a
np:Provenance
.
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_assertion
{
miriam-gene:488
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGNea38b5749eb8ab9c8bda612bcaf6cdc9
sio:SIO_000628
miriam-gene:488
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_provenance
{
dgn-np:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_assertion
dcterms:description
"[A key feature of the failing heart is a decreased content and activity of SERCA2, which is the cause of some of the physiological defects observed in the hypertrophic cardiomyocyte performance that are important during transition of compensated hypertrophy to heart failure.]. 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:16902596
;
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:NP365567.RAIaLjIqX1KuG_Ori2EuIob2M0jSF2NHLpz0SimaWcbP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:34+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" .
}