@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks
> .
@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:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_head
{
this:
np:hasAssertion
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion
;
np:hasProvenance
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance
;
np:hasPublicationInfo
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion
a
np:Assertion
.
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance
a
np:Provenance
.
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGNd05d53d703036a5aa39ec354dbb5991a
sio:SIO_000628
miriam-gene:7439
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_provenance
{
dgn-np:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_assertion
dcterms:description
"[These data confirm the involvement of the VMD2 gene in Best macular dystrophy onset, even in sporadic cases of the disease, pointing out the relevance of molecular analysis in the diagnosis of this degenerative retinal 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:10682987
;
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:NP732241.RAmCsnnD1WkGDrS6B_0P0rbCdgojY7OTM_T5TEGvdr4Ks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}