@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw
> .
@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:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_head
{
this:
np:hasAssertion
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_assertion
;
np:hasProvenance
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_provenance
;
np:hasPublicationInfo
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_assertion
a
np:Assertion
.
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_provenance
a
np:Provenance
.
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_assertion
{
miriam-gene:4313
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN03658b8cc204371723e9f85450646704
sio:SIO_000628
miriam-gene:4313
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_provenance
{
dgn-np:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_assertion
dcterms:description
"[Irrespective of the individual genotype, LOXL1 expression was significantly increased in early PEX stages but was decreased in advanced stages both with and without glaucoma compared with controls, whereas LOX and LOXL2 showed no differences between groups.]. 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:18974306
;
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:NP779080.RAYxfvEcEf0chtzTslL9EbjSQ2W7TvPARUay4tny0G5zw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}