@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_head
{
this:
np:hasAssertion
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion
;
np:hasProvenance
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion
a
np:Assertion
.
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance
a
np:Provenance
.
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion
{
miriam-gene:1137
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN36cf104d046d2afd2f69fbec95548df3
sio:SIO_000628
miriam-gene:1137
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_provenance
{
dgn-np:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_assertion
dcterms:description
"[Understanding of the molecular basis of paroxysmal disorders affecting the central nervous system has been revolutionalized with the identification of mutations in genes for the neurotransmitter receptors, GLRA1 and CHRNA4, and a voltage-gated potassium channel, KCNA1, as causes of inherited neurological disease.]. 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:7620586
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP320203.RAsjqXNtTN8WHZr31lL_NlnOmBEhrz-ZTEKPxejOMbO1Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}