@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I
> .
@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:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_head
{
this:
np:hasAssertion
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_assertion
;
np:hasProvenance
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_provenance
;
np:hasPublicationInfo
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_assertion
a
np:Assertion
.
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_provenance
a
np:Provenance
.
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_assertion
{
miriam-gene:7045
a
ncit:C16612
.
lld:C1832884
a
ncit:C7057
.
dgn-gda:DGN88bffddf704decb2d6d565898f0f0486
sio:SIO_000628
miriam-gene:7045
,
lld:C1832884
;
a
sio:SIO_001121
.
}
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_provenance
{
dgn-np:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_assertion
dcterms:description
"[These findings are consistent with the hypothesis that FHM mutations share the ability of rendering the brain more susceptible to CSD by causing either excessive synaptic glutamate release (FHM1) or decreased removal of K+ and glutamate from the synaptic cleft (FHM2) or excessive extracellular K+ (FHM3).]. 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:17395138
;
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:NP601794.RAItd--9eU8u0l-eW5cf_mItDtOO1raC3UdGljcgpQG_I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:18+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" .
}