@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo
> .
@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:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_head
{
this:
np:hasAssertion
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_assertion
;
np:hasProvenance
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_provenance
;
np:hasPublicationInfo
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_assertion
a
np:Assertion
.
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_provenance
a
np:Provenance
.
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_assertion
{
miriam-gene:776
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN9634e90558827987005663c7048fc217
sio:SIO_000628
miriam-gene:776
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_provenance
{
dgn-np:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_assertion
dcterms:description
"[The determination of the structures of the human CACNL1A2 and CACNLB3 genes should facilitate study of the role of these genes in the development of NIDDM and also other genetic diseases such as long QT syndrome.]. 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:7557998
;
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:NP798739.RApDHfSaqt_iNGhiyxqzjenPbkDeIM5-fgHulWo2I5VGo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}