@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc
> .
@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:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_head
{
this:
np:hasAssertion
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion
;
np:hasProvenance
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance
;
np:hasPublicationInfo
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion
a
np:Assertion
.
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance
a
np:Provenance
.
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion
{
miriam-gene:4855
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN05e62725ded95588e002325218ec2885
sio:SIO_000628
miriam-gene:4855
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_provenance
{
dgn-np:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_assertion
dcterms:description
"[We directly sequenced all 33 exons, the promoter and 3'-untranslated region of NOTCH3 in 195 participants with either coalescent white matter lesions or lacunes and compared the results to 82 randomly selected participants with no focal changes on magnetic resonance images in the Austrian Stroke Prevention Study.]. 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:22006983
;
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:NP260700.RAB66j2V3Dc9w0M9OFY4p6iN_1hHeiwxOC8CZH0SWJ7dc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}