@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_head
{
this:
np:hasAssertion
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_assertion
;
np:hasProvenance
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_provenance
;
np:hasPublicationInfo
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_assertion
a
np:Assertion
.
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_provenance
a
np:Provenance
.
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_assertion
{
miriam-gene:10133
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN888156cb82d9313a229a1ffad99d3ce0
sio:SIO_000628
miriam-gene:10133
,
lld:C0017601
;
a
sio:SIO_001122
.
}
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_provenance
{
dgn-np:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_assertion
dcterms:description
"[ The association of the allelic variation (Met98Lys) in the OPTN gene and the prevalence of POAG and NTG in unrelated Japanese patients suggest that they are involved in the pathogenesis of POAG and NTG.]. 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:15226658
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP86464.RA6dzCQH-UxO3IrCFOGQsGSXhnzgS-dqq3licZ7BZFoGk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}