@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ
> .
@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:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_head
{
this:
np:hasAssertion
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_assertion
;
np:hasProvenance
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_assertion
a
np:Assertion
.
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_provenance
a
np:Provenance
.
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0022336
a
ncit:C7057
.
dgn-gda:DGN2c2ea62d8b494f1f67df196f03f4aafa
sio:SIO_000628
miriam-gene:4397
,
lld:C0022336
;
a
sio:SIO_001121
.
}
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_provenance
{
dgn-np:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_assertion
dcterms:description
"[An Irish family, likely to be part of the same kindred, is also described, in which diagnoses of multiple sclerosis, dementia, corticobasal degeneration and new variant CJD have been considered in affected individuals.]. 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:10506086
;
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:NP583825.RAohHyh4B1zE8ncYfXwi1KgcGPo93c5SWN3mvX0nLaHbQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}