@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM
> .
@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/v3.0.0/void/
> .
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_head
{
this:
np:hasAssertion
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_assertion
;
np:hasProvenance
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_provenance
;
np:hasPublicationInfo
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_assertion
a
np:Assertion
.
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_provenance
a
np:Provenance
.
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_assertion
{
miriam-gene:999
a
ncit:C16612
.
lld:C0017612
a
ncit:C7057
.
dgn-gda:DGN8455a18f6961ead7c4607811f7467e50
sio:SIO_000628
miriam-gene:999
,
lld:C0017612
;
a
sio:SIO_001122
.
}
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_provenance
{
dgn-np:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_assertion
dcterms:description
"[The findings suggest that variants in TNF and TP53 are risk factors for POAG, whereas variants in other studied genes are not major risk factors for POAG, at least in the Chinese population.]. 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:20357201
;
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:NP145892.RA79drQEYGCQegPSrD0Y44tfa2PhzYGh4oYysk0wKchLM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:02+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}