@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE
> .
@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:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_head
{
this:
np:hasAssertion
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_assertion
;
np:hasProvenance
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_provenance
;
np:hasPublicationInfo
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_assertion
a
np:Assertion
.
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_provenance
a
np:Provenance
.
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_assertion
{
miriam-gene:7172
a
ncit:C16612
.
lld:C0023530
a
ncit:C7057
.
dgn-gda:DGN339007176ab2d8b2ba425480b8596279
sio:SIO_000628
miriam-gene:7172
,
lld:C0023530
;
a
sio:SIO_001122
.
}
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_provenance
{
dgn-np:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_assertion
dcterms:description
"[Our work supports the strong evidence that individuals with TPMT variant homozygosity are at high risk of severe neutropenia, whereas TPMT heterozygotes are not at increased risk of ADRs at standard doses of azathioprine.]. 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:21692613
;
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:NP903776.RAz5Jv2AS35SYPXtcDSufFvr6nSgalRv4NAbeVanzPUSE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:33+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" .
}