@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs
> .
@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 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:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_head
{
this:
np:hasAssertion
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_assertion
;
np:hasProvenance
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_provenance
;
np:hasPublicationInfo
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_assertion
a
np:Assertion
.
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_provenance
a
np:Provenance
.
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN72f468b3cf41c7cb2a1c1a8bac288a40
sio:SIO_000628
miriam-gene:2952
,
lld:C0026764
;
a
sio:SIO_001122
.
}
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_provenance
{
dgn-np:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_assertion
dct:description
"[In a case-control study, 90 Australian Caucasians with MM had significantly higher incidences of GST T1 null, PON1 BB and NAT2 slow acetylation genotypes, but no difference in polymorphism frequencies for GST M1, NAT1, and CYP1A1 when compared to 205 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:15136237
;
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:NP42861.RAgN5UjNkdd_mtgdzCllQh9MAKBBD4XSaLHd660pJtBEs130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:19+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}