@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro
> .
@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:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_head
{
this:
np:hasAssertion
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_assertion
;
np:hasProvenance
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_provenance
;
np:hasPublicationInfo
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_assertion
a
np:Assertion
.
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_provenance
a
np:Provenance
.
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_assertion
{
miriam-gene:4016
a
ncit:C16612
.
lld:C0206368
a
ncit:C7057
.
dgn-gda:DGN120c5c5c6fd958fce5273ca72bdbf7e2
sio:SIO_000628
miriam-gene:4016
,
lld:C0206368
;
a
sio:SIO_001121
.
}
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_provenance
{
dgn-np:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_assertion
dcterms:description
"[These results indicate that the G153D LOXL1 variant is significantly associated with an increased risk of pseudoexfoliation and pseudoexfoliation glaucoma in an ethnically diverse patient population from the Northeastern United States.]. 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:18254956
;
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:NP190150.RARdaY6j4V0j1Sw0w9y9al5URnoXvCsOg9yD_GfFLyLro130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}