@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g
> .
@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:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_head
{
this:
np:hasAssertion
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_assertion
;
np:hasProvenance
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_assertion
a
np:Assertion
.
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_provenance
a
np:Provenance
.
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN97439bfcaacc7ea09562836f4adac6d0
sio:SIO_000628
miriam-gene:2950
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_provenance
{
dgn-np:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_assertion
dcterms:description
"[ The gene mutation of GST-Pi exon5 is one of the potential vulnerable factors in leukemogenesis of the Chinese children and the genetic polymorphism of exon6 in Chinese is greatly different from that in other races. The role of the newly discovered variant genotype Asp(147) Try in leukemogenesis remains to be further studied.]. 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:14642067
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP43012.RAZ36CiZmUDZdss1iC9WzGR2QSLP4Fq8-KVBhfp03Tp_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:19+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" .
}