@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo
> .
@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:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_head
{
this:
np:hasAssertion
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_assertion
;
np:hasProvenance
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_provenance
;
np:hasPublicationInfo
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_assertion
a
np:Assertion
.
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_provenance
a
np:Provenance
.
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0339573
a
ncit:C7057
.
dgn-gda:DGNa0e0ddd7fd88aa9dffce82766ea52386
sio:SIO_000628
miriam-gene:1545
,
lld:C0339573
;
a
sio:SIO_001121
.
}
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_provenance
{
dgn-np:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_assertion
dcterms:description
"[Although no major effect of common variation at the CYP1B1 locus on POAG was found, there could be an effect of SNPs tagged by rs162562 and represented on the AGCAGCC haplotype.]. 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:21139974
;
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:NP271376.RAQsUTPtaAD-yiQ6oD4013A9zYL3SG577LK3c8zkQmJDo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}