@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g
> .
@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:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_head
{
this:
np:hasAssertion
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_assertion
;
np:hasProvenance
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_provenance
;
np:hasPublicationInfo
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_assertion
a
np:Assertion
.
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_provenance
a
np:Provenance
.
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_assertion
{
miriam-gene:3579
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGNe7b25c6058650f86ce8e28d24d8aa366
sio:SIO_000628
miriam-gene:3579
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_provenance
{
dgn-np:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_assertion
dcterms:description
"[After controlling for multiple comparisons, single nucleotide polymorphisms (SNPs) from four genes, IL3, IL6R, IL8, IL15, were associated with increased colon cancer risk, and CXCR1 and CXCR2 were significantly associated with increased rectal cancer risk.]. 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:22674296
;
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:NP586098.RAxxB4zIeeGxj_1mXevPjkF__OV5vVbapkRvIXCUNcC8g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}