@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0
> .
@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:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_head
{
this:
np:hasAssertion
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_assertion
;
np:hasProvenance
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_assertion
a
np:Assertion
.
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_provenance
a
np:Provenance
.
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C1855465
a
ncit:C7057
.
dgn-gda:DGNab22b92fa8db5bc65234e2c700ddda96
sio:SIO_000628
miriam-gene:3757
,
lld:C1855465
;
a
sio:SIO_001121
.
}
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_provenance
{
dgn-np:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_assertion
dcterms:description
"[This study documented variability of the clinical expression of STGD in relation to the age of onset of the disease, fundus appearance and the ERG response and allowed to subdivide patients into a severe and a mild phenotype group.]. 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:15942264
;
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:NP802527.RAETS34pj3fStHQ7NYuE9CJJZFlNU8aY5m6fhgvnpEwD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}