@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c
> .
@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:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_head
{
this:
np:hasAssertion
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_assertion
;
np:hasProvenance
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_provenance
;
np:hasPublicationInfo
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_assertion
a
np:Assertion
.
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_provenance
a
np:Provenance
.
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_assertion
{
miriam-gene:4308
a
ncit:C16612
.
lld:C0339535
a
ncit:C7057
.
dgn-gda:DGN8ab8fd5dd8ca6b9deedccec1d5cef650
sio:SIO_000628
miriam-gene:4308
,
lld:C0339535
;
a
sio:SIO_001121
.
}
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_provenance
{
dgn-np:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_assertion
dcterms:description
"[This review covers the significant discoveries on the physiological function and regulatory mechanism of the TRPM1 channel in retinal ON bipolar cells and the association of human TRPM1 mutations with congenital stationary night blindness.]. 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:20846719
;
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:NP708880.RARWdcEa8ZtfivNq4dJPEXrMl5HcvHFDIAahPUVse0n6c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}