@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4
> .
@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:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_head
{
this:
np:hasAssertion
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_assertion
;
np:hasProvenance
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_assertion
a
np:Assertion
.
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_provenance
a
np:Provenance
.
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_assertion
{
miriam-gene:1571
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGN3d8c5a91e06111b052a9fc64fe9c6f49
sio:SIO_000628
miriam-gene:1571
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_provenance
{
dgn-np:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_assertion
dcterms:description
"[Knockdown or downregulation of CYP2E1 might be a therapeutic strategy to control the development of DCM after mutations of cTnT(R141W) or other factors, because DCM is the third most common cause of heart failure and the most frequent cause of heart transplantation.]. 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:22665122
;
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:NP392168.RAQhkWZGCG379eH80LnratGiRLtlaMesT_GnEiWzTQSk4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}