@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI
> .
@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:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_head
{
this:
np:hasAssertion
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_assertion
;
np:hasProvenance
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_assertion
a
np:Assertion
.
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_provenance
a
np:Provenance
.
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C1302401
a
ncit:C7057
.
dgn-gda:DGNf51c28ad5978c6b3741df0d52eabccc3
sio:SIO_000628
miriam-gene:2950
,
lld:C1302401
;
a
sio:SIO_001122
.
}
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_provenance
{
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_assertion
dcterms:description
"[Although with modest limitations and biases, this metaanalysis suggests that EPHX1 Tyr113His and His139Arg, GSTT1, GSTM1, GSTP1 Ile105Val and Ala114Val polymorphisms may be not risk factors for CRA development, while Ser allele of NQO1 Ser187 Pro may be a modest risk factor for CRA development, and may be used with other genetic markers for screening CRA in the future.]. 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:22161138
;
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 .
}
dgn-np:NP946027.RAS7vh7wHoW2UKGrjTvFoLMOHm_oVyQUyBAVaJQxhLmvI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:53+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}