@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg
> .
@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:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_head
{
this:
np:hasAssertion
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_assertion
;
np:hasProvenance
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_provenance
;
np:hasPublicationInfo
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_assertion
a
np:Assertion
.
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_provenance
a
np:Provenance
.
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_assertion
{
miriam-gene:7137
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGNda532b8a303dcbe372cda288e45b3998
sio:SIO_000628
miriam-gene:7137
,
lld:C0878544
;
a
sio:SIO_001121
.
}
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_provenance
{
dgn-np:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_assertion
dcterms:description
"[In this study, comprehensive screening of TNNI3 was performed in 36 consented autopsy cases diagnosed as CM, in order to evaluate the prevalence of gene mutations in sudden death caused by CM.]. 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:20817590
;
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:NP829806.RA6isSv_VI7dCu3aOI8Hz-D7ThiragXScLDJf1wfxktyg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}