@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_head
{
this:
np:hasAssertion
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion
;
np:hasProvenance
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion
a
np:Assertion
.
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance
a
np:Provenance
.
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion
{
miriam-gene:3736
a
ncit:C16612
.
lld:C1720189
a
ncit:C7057
.
dgn-gda:DGNe0c2d0cea21cff910cd760ab35ea6622
sio:SIO_000628
miriam-gene:3736
,
lld:C1720189
;
a
sio:SIO_001121
.
}
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_provenance
{
dgn-np:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_assertion
dcterms:description
"[Taken together, these results show that the different mutations in Kv1.1 affect channel function and indicate that both dominant negative effects and haplotype insufficiency may result in the symptoms of EA.]. 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:9526001
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP521314.RAy61UHSdPC9Cs7JMoGetwmJ5gtEWjlOMVCyQWu9G4G1s130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:48+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}