@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw
> .
@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:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_head
{
this:
np:hasAssertion
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_assertion
;
np:hasProvenance
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_assertion
a
np:Assertion
.
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_provenance
a
np:Provenance
.
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_assertion
{
miriam-gene:4854
a
ncit:C16612
.
lld:C0042373
a
ncit:C7057
.
dgn-gda:DGNfa7a47f70cdd68aeeabbc06fc9316b44
sio:SIO_000628
miriam-gene:4854
,
lld:C0042373
;
a
sio:SIO_001121
.
}
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_provenance
{
dgn-np:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_assertion
dcterms:description
"[Therefore, we propose to consider a replacement for the name CADASIL that better reflects the morphological picture of the disease like, for example, cerebral autosomal dominant vasculopathy with subcortical infarcts and leukoencephalopathy (CADVaSIL) or, to preserve the commonly known acronym, cerebral autosomal dominant angiopathy with subcortical infarcts and leukoencephalopathy.]. 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:15068168
;
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:NP780604.RAuUwRIcLjvxhOiRrYYqMG371M5bxQvU3EC8Y9oV8uZBw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}