@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0
> .
@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:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_head
{
this:
np:hasAssertion
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_assertion
;
np:hasProvenance
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_provenance
;
np:hasPublicationInfo
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_assertion
a
np:Assertion
.
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_provenance
a
np:Provenance
.
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C3178801
a
ncit:C7057
.
dgn-gda:DGN81e8cc01f59720bd0f5d971f0a959cf8
sio:SIO_000628
miriam-gene:4854
,
lld:C3178801
;
a
sio:SIO_001121
.
}
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_provenance
{
dgn-np:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_assertion
dcterms:description
"[The identification of NOTCH3 mutations in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) and of TREX1 mutations in retinal vasculopathy with cerebral leukodystrophy (RVCL) have led to new insights on lacunar stroke and small-vessel disease.]. 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:22113147
;
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:NP941393.RAynU-9eVB-Dgcuq8B37u7vxn2S_ncqfRzw4sDJF48WY0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:51+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: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" .
}