@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs
> .
@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:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_assertion
;
np:hasProvenance
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_provenance
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np:hasPublicationInfo
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_assertion
a
np:Assertion
.
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_provenance
a
np:Provenance
.
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:6256
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN19668131e6c74624c82e6fafcb806483
sio:SIO_000628
miriam-gene:6256
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_provenance
{
dgn-np:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_assertion
dcterms:description
"[Employing a discordant-sibship case-control design, we examined the association between single nucleotide polymorphisms (SNPs) in RXRA and CASR and risk for colorectal cancer overall and by colorectal subsite and microsatellite instability (MSI) status using data from the Colon Cancer Family Registry.]. 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:20558521
;
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:NP870385.RAdRRbIecY4JHfED0JIfhwZ2jSKo2HpHWyc3wNwu0Hogs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
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
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}