@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw
> .
@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:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_head
{
this:
np:hasAssertion
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_assertion
;
np:hasProvenance
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_provenance
;
np:hasPublicationInfo
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_assertion
a
np:Assertion
.
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_provenance
a
np:Provenance
.
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_assertion
{
miriam-gene:231
a
ncit:C16612
.
lld:C0038325
a
ncit:C7057
.
dgn-gda:DGN0d3f0d38cb1f3a43402b085d3e2bbf8d
sio:SIO_000628
miriam-gene:231
,
lld:C0038325
;
a
sio:SIO_001121
.
}
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_provenance
{
dgn-np:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_assertion
dcterms:description
"[In the field of severe cutaneous adverse drug reactions (cutaneous ADR) such as Stevens-Johnson syndrome (SJS), toxic epidermal necrolysis (TEN), and drug-induced hypersensitivity syndrome (DHIS) or drug rash with eosinophilia and systemic symptoms (DRESS), major advances have recently been gained through studies of an association between HLA alleles and drug hypersensitivity induced by specific drugs.]. 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:21342226
;
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:NP614444.RAe26kbHKYGncVq37FEIiMqLpZ9dKnLriojDXA0M9jXTw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}