@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM
> .
@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:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_head
{
this:
np:hasAssertion
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion
;
np:hasProvenance
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance
;
np:hasPublicationInfo
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion
a
np:Assertion
.
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance
a
np:Provenance
.
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion
{
miriam-gene:6649
a
ncit:C16612
.
lld:C0151744
a
ncit:C7057
.
dgn-gda:DGN4c5d0077e2e449b108217264c4e20cb7
sio:SIO_000628
miriam-gene:6649
,
lld:C0151744
;
a
sio:SIO_001122
.
}
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_provenance
{
dgn-np:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_assertion
dcterms:description
"[Substitution of arginine by glycine at amino acid 213 (R213G) of its HBD was first identified in patients with heart failure, followed by many studies that focused on the role of this variant (SOD3(R213G)) in ischemic heart disease and cardiovascular disease.]. 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:25927599
;
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:NP1281568.RAoZlcZbUn4T_c4vk_OqB9gwAb0wniRPghP5DlDYaEGbM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:27+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" .
}