@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU
> .
@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:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_head
{
this:
np:hasAssertion
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_assertion
;
np:hasProvenance
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_provenance
;
np:hasPublicationInfo
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_assertion
a
np:Assertion
.
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_provenance
a
np:Provenance
.
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGNd9b19d011a4172e0a96524a783771e2a
sio:SIO_000628
miriam-gene:2944
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_provenance
{
dgn-np:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_assertion
dcterms:description
"[The frequency of GSTM1 positive individuals was significantly higher in MT cataracts followed by NC, CC and PSC types with corresponding decrease in the GSTM1 null genotypes as compared to controls.]. 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:22446016
;
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:NP879506.RA_p90PRRmsss1NiSyxJFrH7zJleIk2tF9CIVTsiQ36XU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}