@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0
> .
@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:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_head
{
this:
np:hasAssertion
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion
;
np:hasProvenance
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion
a
np:Assertion
.
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance
a
np:Provenance
.
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN1742ec0f5e91961f38706ebb9d3c3733
sio:SIO_000628
miriam-gene:1543
,
lld:C0026764
;
a
sio:SIO_001122
.
}
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_provenance
{
dgn-np:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_assertion
dcterms: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:NP46119.RAW8hU9vEYioEpW6jvT1jSbcb9fO9jwHRGeNtnlPrYYr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}