@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY
> .
@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:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_head
{
this:
np:hasAssertion
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_assertion
;
np:hasProvenance
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_provenance
;
np:hasPublicationInfo
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_assertion
a
np:Assertion
.
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_provenance
a
np:Provenance
.
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_assertion
{
miriam-gene:10133
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN90b804501462ba42425ca6597dd20dc4
sio:SIO_000628
miriam-gene:10133
,
lld:C0017601
;
a
sio:SIO_001122
.
}
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_provenance
{
dgn-np:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_assertion
dcterms:description
"[Since NTG is reported to be the most common form of glaucoma in Japan, and to identify if the OPTN gene plays a role in POAG, the DNAs from 148 unrelated Japanese patients with NTG, 165 patients with POAG and 196 unrelated controls who were not suffering glaucoma were investigated by appropriate genotyping techniques.]. 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:12811537
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53421.RAJLQgOx72cJiBO9S2tncUkaOhvY5ze_J1Nb73fUB5_ZY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}