@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM
> .
@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:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_head
{
this:
np:hasAssertion
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_assertion
;
np:hasProvenance
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_provenance
;
np:hasPublicationInfo
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_assertion
a
np:Assertion
.
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_provenance
a
np:Provenance
.
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_assertion
{
miriam-gene:4126
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNdca1f03b95a72445a1ff9e65e24a1620
sio:SIO_000628
miriam-gene:4126
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_provenance
{
dgn-np:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_assertion
dcterms:description
"[In this study, we investigated the relationship of a polymorphic CA repeat in MANBA gene with CRC risk in 152 Swedish CRC patients and 441 Swedish controls, and 196 Chinese CRC patients and 577 Chinese controls, as well as the clinicopathologic significance of this polymorphism on CRC patients, by using capillary electrophoresis.]. 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:17899454
;
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:NP85862.RAYKpo2ph-URGLVuOV9-irI4IMkGaGVVqV-9vW-rQvfdM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}