@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI
> .
@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:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_head
{
this:
np:hasAssertion
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_assertion
;
np:hasProvenance
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_provenance
;
np:hasPublicationInfo
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_assertion
a
np:Assertion
.
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_provenance
a
np:Provenance
.
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_assertion
{
miriam-gene:2153
a
ncit:C16612
.
lld:C0035326
a
ncit:C7057
.
dgn-gda:DGNcf4e26bfe4e4b3620be49eb5d8f84100
sio:SIO_000628
miriam-gene:2153
,
lld:C0035326
;
a
sio:SIO_001122
.
}
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_provenance
{
dgn-np:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_assertion
dcterms:description
"[ Our data indicate that the prevalences of the investigated gene polymorphisms do not differ significantly in patients with BRVO and control subjects. This suggests that these polymorphisms are not major risk factors for BRVO.]. 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:16157382
;
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:NP44395.RAwpI5pQSKYyyvh6qO00quEX71dVLPJ5okiPkUErJKOgI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}