@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo
> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_assertion
a
np:Assertion
.
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_provenance
a
np:Provenance
.
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0220669
a
ncit:C7057
.
dgn-gda:DGNbbf7cbcfa3f3e0c4ead75a923ad192e5
sio:SIO_000628
miriam-gene:3785
,
lld:C0220669
;
a
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.
}
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_provenance
{
dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_assertion
dcterms:description
"[KCNQ2-5 channels are predominantly expressed in neurons and are important determinants of cellular excitability, as indicated by the occurrence of human genetic mutations in KCNQ channels that underlie inheritable disorders including, in the case of KCNQ2/3, the syndrome of benign familial neonatal convulsions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:22220513
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP951055.RAnlFeJuPWTPxSiCbBbjHbvPboahaA0W7075crLkJjDbo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:56+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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
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"v4.0.0" .
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