@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A
> .
@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:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_head
{
this:
np:hasAssertion
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_assertion
;
np:hasProvenance
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_provenance
;
np:hasPublicationInfo
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_assertion
a
np:Assertion
.
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_provenance
a
np:Provenance
.
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_assertion
{
miriam-gene:1282
a
ncit:C16612
.
lld:C0023520
a
ncit:C7057
.
dgn-gda:DGNa7ff965486bc1ef5aa3d833fd3e0700a
sio:SIO_000628
miriam-gene:1282
,
lld:C0023520
;
a
sio:SIO_001121
.
}
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_provenance
{
dgn-np:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_assertion
dcterms:description
"[With emphasis on cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), we review the molecular pathogenesis of recently characterized disorders including cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), retinal vasculopathy with cerebral leukodystrophy (RVCL) and the Collagen type IV, alpha 1 (COL4A1)-related disorders.]. 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:21062344
;
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:NP206620.RAwFXFRHA6aHDoTc63fkh7lYZKwGDE0K-wwCBAnWi6o7A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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: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" .
}