@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0
> .
@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:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_head
{
this:
np:hasAssertion
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_assertion
;
np:hasProvenance
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_assertion
a
np:Assertion
.
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_provenance
a
np:Provenance
.
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_assertion
{
miriam-gene:3785
a
ncit:C16612
.
lld:C0220669
a
ncit:C7057
.
dgn-gda:DGN2e15436da6cd1320d7850e6200c6554f
sio:SIO_000628
miriam-gene:3785
,
lld:C0220669
;
a
sio:SIO_001121
.
}
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_provenance
{
dgn-np:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_assertion
dcterms:description
"[Interestingly, in the majority of the cases, the initial epileptic features of these patients were comparable to those previously described in the case of benign familial neonatal epilepsy (BFNE) also caused by KCNQ2 mutations.]. 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:23692823
;
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:NP1079398.RAF7kFQ_o07CivUW7c_C1RKYbZTFTdImGEMbvSO29eew0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:55+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" .
}