@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_assertion
a
np:Assertion
.
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_provenance
a
np:Provenance
.
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_assertion
{
miriam-gene:4089
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNa244df5662d09d4d5e4c29c403ad81c3
sio:SIO_000628
miriam-gene:4089
,
lld:C1527249
;
a
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.
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dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_provenance
{
dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_assertion
dcterms:description
"[Here, in this study we aimed to investigate the role of SMAD4 gene aberrations in the pathogenesis of CRC in Kashmir valley and to correlate it with various clinicopathological variables and KRAS mutant genotype.]. 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:20565773
;
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 .
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dgn-np:NP199355.RAowgKHUP90tiy-8z3N9FpGRfus8jU9GbcHv-NgP5weio130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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