@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g
> .
@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/
> .
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_head
{
this:
np:hasAssertion
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_provenance
a
np:Provenance
.
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_publicationInfo
a
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.
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dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_assertion
{
miriam-gene:29110
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN9582524752495b949fce042655352ea5
sio:SIO_000628
miriam-gene:29110
,
lld:C0017601
;
a
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.
}
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_provenance
{
dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_assertion
dcterms:description
"[Together, these data link the duplication of genes on chromosome 12q14 with familial NTG and suggest that an extra copy of the encompassed TBK1 gene is likely responsible for these cases of glaucoma.]. 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:21447600
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP883096.RAXRTlfNFzooHSthVLDpe1Unc8pHObK6pfK_Xvdeiv36g130_publicationInfo
{
this:
dcterms:created
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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
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prv:usedData
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<
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
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<
http://orcid.org/0000-0003-0169-8159
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pav:version
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"v4.0.0" .
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