@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M
> .
@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:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_head
{
this:
np:hasAssertion
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_assertion
;
np:hasProvenance
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_provenance
;
np:hasPublicationInfo
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_assertion
a
np:Assertion
.
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_provenance
a
np:Provenance
.
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_assertion
{
miriam-gene:10205
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN0d8a9cd39e5a276dae88a959723bac53
sio:SIO_000628
miriam-gene:10205
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_provenance
{
dgn-np:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_assertion
dcterms:description
"[Although the characteristic symptoms of EVA including fluctuating HL and repetitive vertigo were not seen in the patient, further studies are needed to clarify the association between EVA and such symptoms.]. 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:21254961
;
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:NP215538.RABohwlBXe00kSxgyvL9MbUgaScMAfGi4B5zKsBNizP4M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}