@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ
> .
@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/v4.0.0/void/
> .
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_head
{
this:
np:hasAssertion
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_assertion
;
np:hasProvenance
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_assertion
a
np:Assertion
.
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_provenance
a
np:Provenance
.
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0751587
a
ncit:C7057
.
dgn-gda:DGNfce0dc56ba5dfab373ec07c51dfdc4fd
sio:SIO_000628
miriam-gene:4854
,
lld:C0751587
;
a
sio:SIO_001121
.
}
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_provenance
{
dgn-np:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_assertion
dcterms:description
"[To investigate the Notch 3 mutation spectrum in Arab patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy CADASIL, which is an inherited cerebrovascular disease characterized by recurrent subcortical ischemic stroke starting in the third or fourth decade.]. 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:18626519
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP682108.RAmZV2HyKH8WII0A3FAKsLgykaUDCMR3VYL8TfT5Su8WQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:54+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}