@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I
> .
@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:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_head
{
this:
np:hasAssertion
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_assertion
;
np:hasProvenance
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_provenance
;
np:hasPublicationInfo
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_assertion
a
np:Assertion
.
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_provenance
a
np:Provenance
.
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_assertion
{
miriam-gene:10133
a
ncit:C16612
.
lld:C0339573
a
ncit:C7057
.
dgn-gda:DGN77ba5a81d63f42ffd423997981c40ab7
sio:SIO_000628
miriam-gene:10133
,
lld:C0339573
;
a
sio:SIO_001122
.
}
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_provenance
{
dgn-np:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_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:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP450378.RAvweD1xEkeSgLEkJGQWdjs13sM4KRyXTyaMUkSbMPY6I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:09+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
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;
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" .
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pav:version
"v4.0.0" .
}