@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU
> .
@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:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_assertion
;
np:hasProvenance
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_provenance
;
np:hasPublicationInfo
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_assertion
a
np:Assertion
.
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_provenance
a
np:Provenance
.
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNb96b6f16095d0773091963e59a30a313
sio:SIO_000628
miriam-gene:4683
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_provenance
{
dgn-np:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_assertion
dcterms:description
"[To assess whether NBN 657del5 associates with an increased risk of sporadic colorectal cancer, we have screened 771 colorectal cancer patients, 614 controls with negative colonoscopy and 818 healthy blood donors from the Czech Republic.]. 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:19393249
;
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:NP69152.RAN7KqfMarFWN_GsQXCzZWCdEJi61ApkRNfTWcs-NHXkU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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" .
}