@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI
> .
@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:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_head
{
this:
np:hasAssertion
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_assertion
;
np:hasProvenance
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_provenance
;
np:hasPublicationInfo
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_assertion
a
np:Assertion
.
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_provenance
a
np:Provenance
.
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_assertion
{
miriam-gene:7172
a
ncit:C16612
.
lld:C0013182
a
ncit:C7057
.
dgn-gda:DGNb3c73068f8f63302e6871d94544fab34
sio:SIO_000628
miriam-gene:7172
,
lld:C0013182
;
a
sio:SIO_001122
.
}
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_provenance
{
dgn-np:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_assertion
dcterms:description
"[The positive predictive value of genotyping was low, but the likelihood ratio for developing either haematological or hepatotoxicity by identifying TPMT heterozygosity, was 9.75. In our patient population this translates into an improvement from a pre-test probability of developing haematological or hepatotoxicity of 11%, to a post-test level of 50%. Heterozygous patients may then be targeted for a more `tailored` increase in dosing and regular laboratory monitoring.]. 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:15792824
;
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:NP58847.RAOpdrnxIhC6_bc4OEm1yx_SxNiLgRVZp9fkUA3de30FI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}