@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o
> .
@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:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_head
{
this:
np:hasAssertion
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_assertion
;
np:hasProvenance
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_assertion
a
np:Assertion
.
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_provenance
a
np:Provenance
.
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_assertion
{
miriam-gene:2068
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN43a86e300f7ce625fdeefdfbc7bafa5d
sio:SIO_000628
miriam-gene:2068
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_provenance
{
dgn-np:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_assertion
dcterms:description
"[We analyzed 20 germline polymorphisms in 10 genes (TS, MTHFR, ERCC1, XPD, XRCC1, ABCC2, AGXT, GSTP1, GSTT1 and GSTM1) from prospectively enrolled 292 Korean patients treated with adjuvant oxaliplatin plus leucovorin plus 5-fluorouracil (FOLFOX) for colon cancer.]. 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:23314736
;
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:NP639430.RAyivwEml5wrwXLGDDgn4_qlMsHUNkWn5GgWP9A9mkk7o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:25+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" .
}