@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU
> .
@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:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_head
{
this:
np:hasAssertion
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion
;
np:hasProvenance
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance
;
np:hasPublicationInfo
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion
a
np:Assertion
.
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance
a
np:Provenance
.
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion
{
miriam-gene:79612
a
ncit:C16612
.
lld:C0015230
a
ncit:C7057
.
dgn-gda:DGN3cf95e99799628da22b3fd030a81d5bc
sio:SIO_000628
miriam-gene:79612
,
lld:C0015230
;
a
sio:SIO_001121
.
}
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_provenance
{
dgn-np:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_assertion
dcterms:description
"[Despite careful medical record review and full resequencing of the NAT2 coding region, we found no association of NAT2 coding alleles with sulfonamide hypersensitivity (predominantly cutaneous eruptions) in this adult Caucasian population.]. 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:22850190
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP884357.RARRNh6gNHAsipdwkke5kRxVF-3C2yXOy3P81VO3QlSQU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:00+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" .
}