@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE
> .
@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:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_head
{
this:
np:hasAssertion
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_assertion
;
np:hasProvenance
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_provenance
;
np:hasPublicationInfo
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_assertion
a
np:Assertion
.
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_provenance
a
np:Provenance
.
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_assertion
{
miriam-gene:9429
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNb86825672ca24fe79473a4342025b993
sio:SIO_000628
miriam-gene:9429
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_provenance
{
dgn-np:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_assertion
dcterms:description
"[This study provides a platform to evaluate pharmacogenetic predictors of response or severe adverse events in advanced CRC. Pharmacogenetic studies can be conducted in multicenter trials, and our findings demonstrate that with continued research, clinical application is practical.]. 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:20530282
;
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:NP69557.RAdTjw5p4iIIQpHdjJiVVnhhXGaqxGZMTO1oEP790sLAE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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: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" .
}