@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4
> .
@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:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_head
{
this:
np:hasAssertion
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_assertion
;
np:hasProvenance
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_provenance
;
np:hasPublicationInfo
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_assertion
a
np:Assertion
.
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_provenance
a
np:Provenance
.
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNf1cd32317da28d153b2771d7f599156c
sio:SIO_000628
miriam-gene:3785
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_provenance
{
dgn-np:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_assertion
dcterms:description
"[Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in patients affected with early onset epilepsies with wide phenotypic heterogeneity, ranging from benign familial neonatal seizures (BFNS) to epileptic encephalopathy with cognitive impairment, drug resistance, and characteristic electroencephalography (EEG) and neuroradiologic features.]. 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:25524373
;
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:NP1249444.RAjoYMzob_Zhn2MZy5EiF4l9HnFo34a9MRblaZhgX7ah4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:12+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" .
}