@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g
> .
@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:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_head
{
this:
np:hasAssertion
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_assertion
;
np:hasProvenance
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_provenance
;
np:hasPublicationInfo
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_assertion
a
np:Assertion
.
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_provenance
a
np:Provenance
.
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0152439
a
ncit:C7057
.
dgn-gda:DGNa7d475c70215dbfb762c5f14a9a0fbc1
sio:SIO_000628
miriam-gene:3757
,
lld:C0152439
;
a
sio:SIO_001121
.
}
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_provenance
{
dgn-np:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_assertion
dcterms:description
"[The two brothers with ophthalmic disease were evaluated with color fundus photography, fluorescein angiography, optical coherence tomography (OCT), molecular genetic study (Group VI of Retinoschisis Consortium), pattern visual evoked potential (PVEP), and full field ERG.]. 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:16167295
;
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:NP617368.RAw2aByDr4xPAoZT1CB9BnuChLu1eYSrB_ARHU1Wke00g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}