@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_assertion
a
np:Assertion
.
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_provenance
a
np:Provenance
.
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_assertion
{
miriam-gene:4016
a
ncit:C16612
.
lld:C0017612
a
ncit:C7057
.
dgn-gda:DGN7847fef96f40714d69dedbd74b052aa3
sio:SIO_000628
miriam-gene:4016
,
lld:C0017612
;
a
sio:SIO_001122
.
}
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_provenance
{
dgn-np:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_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:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP118578.RAbEq1rTw8uvonZX4b3sX19GjsxiY5hxU1cc91HxiGGVI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:41+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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" .
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