@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE
> .
@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:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_head
{
this:
np:hasAssertion
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_assertion
;
np:hasProvenance
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_provenance
;
np:hasPublicationInfo
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_assertion
a
np:Assertion
.
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_provenance
a
np:Provenance
.
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_assertion
{
miriam-gene:570
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN45494e628b742f4b90ebedb0c84baea4
sio:SIO_000628
miriam-gene:570
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_provenance
{
dgn-np:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_assertion
dcterms:description
"[In the present study, we analyzed the type (insertions/deletions), size, and frequency of mutations occurring at three BAT and three dinucleotide markers in CRC and EC, to elucidate whether it is possible to establish different MSI profiles in carcinomas of different tissue origin.]. 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:19373783
;
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:NP629763.RATk_K8iRjAH0qfmTFWcfx6t3434JGC_NjlQs_tnPOjxE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}