@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI
> .
@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/v3.0.0/void/
> .
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_head
{
this:
np:hasAssertion
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_assertion
;
np:hasProvenance
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_assertion
a
np:Assertion
.
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_provenance
a
np:Provenance
.
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0270612
a
ncit:C7057
.
dgn-gda:DGNe918e3abef6ce18e9baee3ff72c622d8
sio:SIO_000628
miriam-gene:4854
,
lld:C0270612
;
a
sio:SIO_001122
.
}
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_provenance
{
dgn-np:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_assertion
dcterms:description
"[a readily usable genetic test for CADASIL has been devised that was used to determine allele frequencies in well characterised cohorts of sporadic stroke and dementia patients.The data suggest that despite the clinical resemblance, CADASIL is not a common]. 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:11032621
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP67435.RAtrxFXSDDjVgx5Jmo3GBoCFitSOqXri4hJ--_U1snHTI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:17+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}