@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y
> .
@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:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_head
{
this:
np:hasAssertion
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_assertion
;
np:hasProvenance
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_assertion
a
np:Assertion
.
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_provenance
a
np:Provenance
.
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_assertion
{
miriam-gene:773
a
ncit:C16612
.
lld:C0011581
a
ncit:C7057
.
dgn-gda:DGNf120591f85eec628e47c3684c305593b
sio:SIO_000628
miriam-gene:773
,
lld:C0011581
;
a
sio:SIO_001121
.
}
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_provenance
{
dgn-np:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_assertion
dcterms:description
"[The mutated FHM genes code for ion transport proteins that animal and cellular studies have associated with disturbed ion homeostasis, altered cellular excitability, neurotransmitter release, and decreased threshold for cortical spreading depression.]. 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:20727009
;
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:NP777900.RAcJ8Q8mwgs_PAEqxvan3BNSXOfFz_89FxHUYJYEMZS6Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}