@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ
> .
@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:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_head
{
this:
np:hasAssertion
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_assertion
;
np:hasProvenance
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_assertion
a
np:Assertion
.
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_provenance
a
np:Provenance
.
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGNfbb99338f0d53e21d94375d9cf535f66
sio:SIO_000628
miriam-gene:4360
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_provenance
{
dgn-np:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_assertion
dcterms:description
"[The purpose of this study was to examine the prognostic and oxaliplatin predictive value of mismatch repair (MMR) status and common hot spot mutations, which we previously identified in stage II and III 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:23045248
;
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:NP185895.RAiJL9WL1yvVIVRKHGrzGVGJf7JCayFXxFGTm25kPdZfQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}