@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434
> .
@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:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_head
{
this:
np:hasAssertion
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_assertion
;
np:hasProvenance
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_provenance
;
np:hasPublicationInfo
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_assertion
a
np:Assertion
.
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_provenance
a
np:Provenance
.
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_assertion
{
miriam-gene:6271
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGNdf7af656bf13b67b4aa3720352fc0701
sio:SIO_000628
miriam-gene:6271
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_provenance
{
dgn-np:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_assertion
dcterms:description
"[Indeed, the possibility that S100 proteins might contribute to heart and vascular diseases was first suggested by the discovery of distinctive patterns of S100 expression in healthy and diseased hearts and vasculature from humans and animal heart failure (HF) models.]. 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:19538970
;
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:NP304427.RA5_hUTKgDuBFGtssiYBLSLsarqAIPV-orVwSE4aJr434130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}