@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84
> .
@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/
> .
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_head
{
this:
np:hasAssertion
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_assertion
;
np:hasProvenance
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_provenance
;
np:hasPublicationInfo
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_assertion
a
np:Assertion
.
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_provenance
a
np:Provenance
.
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0270851
a
ncit:C7057
.
dgn-gda:DGN0aa87721877b54d29017c619a93c99e8
sio:SIO_000628
miriam-gene:3785
,
lld:C0270851
;
a
sio:SIO_001121
.
}
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_provenance
{
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_assertion
dcterms:description
"[The importance of ionic channels as cause of epilepsies was further demonstrated with the identification of the association between the benign neonatal epilepsy and mutations in genes coding for potassium channel subunits (KCNQ2, KCNQ3).]. 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:11690625
;
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 .
}
dgn-np:NP335058.RAVW9_KFvHU8sG82E_8wl8Cvm7LgBD3XgIA2i9KhOip84130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:17+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}