@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs
> .
@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:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_head
{
this:
np:hasAssertion
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_assertion
;
np:hasProvenance
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_assertion
a
np:Assertion
.
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_provenance
a
np:Provenance
.
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_assertion
{
miriam-gene:1462
a
ncit:C16612
.
lld:C0339540
a
ncit:C7057
.
dgn-gda:DGNbca47a499d461c950dbb0d4295c71cc0
sio:SIO_000628
miriam-gene:1462
,
lld:C0339540
;
a
sio:SIO_001121
.
}
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_provenance
{
dgn-np:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_assertion
dcterms:description
"[Wagner syndrome (WS) is an autosomal dominant vitreoretinopathy affecting various ocular features and is caused by mutations in the canonical splice sites of the VCAN gene, which encodes the large chondroitin sulfate proteoglycan, versican.]. 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:22739342
;
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:NP487764.RAOh__sGopYA-4tXVL0-EbAAdDQDdOVQi-4D83ftZhtIs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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: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" .
}