@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE
> .
@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:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_head
{
this:
np:hasAssertion
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion
;
np:hasProvenance
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion
a
np:Assertion
.
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance
a
np:Provenance
.
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion
{
miriam-gene:114327
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN16fda4dc254c20ff19798973801dcd38
sio:SIO_000628
miriam-gene:114327
,
lld:C0014544
;
a
sio:SIO_001122
.
}
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_provenance
{
dgn-np:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_assertion
dcterms:description
"[Public databases also show that the EFHC1 P77T-R221H JME haplotype is present in unphenotyped West African ancestry populations, and we show that it can be found at appreciable frequency in healthy individuals with no family history of epilepsy.]. 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:25489633
;
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:NP1246360.RAsrRa04QiX4Cyw1ssdc5omM37kIGph5Rt4KddVeYCwFE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:10+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" .
}