@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w
> .
@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:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_head
{
this:
np:hasAssertion
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_assertion
;
np:hasProvenance
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_provenance
;
np:hasPublicationInfo
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_assertion
a
np:Assertion
.
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_provenance
a
np:Provenance
.
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN807c16be0a038d64d1bb7dbfa2b87e4f
sio:SIO_000628
miriam-gene:2952
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_provenance
{
dgn-np:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_assertion
dcterms:description
"[We excluded patients and controls with cataract or past history of cataract surgery, asthma, past history of malignancy, cardiovascular disease that on medication and known cases of glaucoma, because these traits were associated with GSTM1 and/or GSTT1 polymorphisms.]. 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:21701824
;
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:NP774166.RALxMMq4c0lQ8Pa4t18q8TK2ym53T_5YcQ0yHwos8O65w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}