@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0
> .
@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:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_head
{
this:
np:hasAssertion
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_assertion
;
np:hasProvenance
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_provenance
;
np:hasPublicationInfo
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_assertion
a
np:Assertion
.
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_provenance
a
np:Provenance
.
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_assertion
{
miriam-gene:220202
a
ncit:C16612
.
lld:C0017612
a
ncit:C7057
.
dgn-gda:DGN9b72bccfb816554de275e4d42780754a
sio:SIO_000628
miriam-gene:220202
,
lld:C0017612
;
a
sio:SIO_001121
.
}
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_provenance
{
dgn-np:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_assertion
dcterms:description
"[This study was performed to determine to what extent variants within established genes (MYOC, OPTN, and WDR36) and newly identified common genetic variants (ATOH7, CDKN2B, and SIX1) contribute to the risk of OAG.]. 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:21872936
;
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:NP469416.RAIUKWJSyjXTwwT_PI9Q9eQwrQfGpH4rjWKjx49tyKoO0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}