@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c
> .
@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:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_head
{
this:
np:hasAssertion
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_assertion
;
np:hasProvenance
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_provenance
;
np:hasPublicationInfo
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_assertion
a
np:Assertion
.
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_provenance
a
np:Provenance
.
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0852949
a
ncit:C7057
.
dgn-gda:DGN31de7380a4797a055f3dec11c2f83081
sio:SIO_000628
miriam-gene:4854
,
lld:C0852949
;
a
sio:SIO_001121
.
}
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_provenance
{
dgn-np:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_assertion
dcterms:description
"[CADASIL, however, may be diagnosed well before the first stroke on the basis of characteristic white matter hyperintensities upon magnetic resonance imaging and presence of pathognomonic granular osmiophilic material in arterial walls, including dermal arteries, since the arteriopathy is generalized.]. 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:12146805
;
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:NP236803.RAEKVym4Rgf47RopiI4UDxRQeiMx-QEr2qZ3EYcH74q_c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}