@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0
> .
@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:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_head
{
this:
np:hasAssertion
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion
;
np:hasProvenance
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance
;
np:hasPublicationInfo
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion
a
np:Assertion
.
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance
a
np:Provenance
.
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion
{
miriam-gene:1565
a
ncit:C16612
.
lld:C0013182
a
ncit:C7057
.
dgn-gda:DGN96f89211e0446652ed29f3da3f696908
sio:SIO_000628
miriam-gene:1565
,
lld:C0013182
;
a
sio:SIO_001122
.
}
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_provenance
{
dgn-np:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_assertion
dcterms:description
"[ In this investigation geriatric patients showed a high rate of ADRs. However, no association between the ADR rate and the patients' genotype could be detected, which most likely was a result of the small number of patient samples analysed.Although prophylactic genotyping would have not prevented ADRs in this pilot study, physicians nevertheless have to be aware of potential genetic mutations in patients with polypharmacy.]. 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:15813658
;
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:NP60055.RAUMq-hJE9QdMSeRkVBnzoJhcUTUL-cJotLuZIrGc5Ou0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}