@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E
> .
@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:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_head
{
this:
np:hasAssertion
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_assertion
;
np:hasProvenance
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_assertion
a
np:Assertion
.
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_provenance
a
np:Provenance
.
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_assertion
{
miriam-gene:358
a
ncit:C16612
.
lld:C0017612
a
ncit:C7057
.
dgn-gda:DGN90ce7d924a6a15f6b9d5c5d5dce2e5e3
sio:SIO_000628
miriam-gene:358
,
lld:C0017612
;
a
sio:SIO_001122
.
}
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_provenance
{
dgn-np:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_assertion
dcterms:description
"[There was no association between common sequence variants in the AQP1 or SLC4A10 genes and POAG in the Caucasian population. This is the first study to investigate the association between these two candidate genes and increased risk for POAG.]. 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:20101282
;
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:NP85493.RAfB-tdOKMzPaL1DdMSxph7M0bhnlTv6PoFPQrNTUnb3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}