@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48
> .
@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:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_head
{
this:
np:hasAssertion
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_assertion
;
np:hasProvenance
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_provenance
;
np:hasPublicationInfo
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_assertion
a
np:Assertion
.
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_provenance
a
np:Provenance
.
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_assertion
{
miriam-gene:50639
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGN6ce0ba7e3b205a1d8dace61dcd6806a5
sio:SIO_000628
miriam-gene:50639
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_provenance
{
dgn-np:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_assertion
dcterms:description
"[We found that 5' secretor haplotypes known to correlate with moderate and low MBL serum levels exhibited associations with increased risk of colon cancer in African Americans, specifically as driven by two haplotypes, LYPA and LYQC, relative to the referent HYPA haplotype (LYPA: OR, 2.60; 95% CI, 1.33-5.08 and LYQC: OR, 2.28; 95% CI, 1.20-4.30).]. 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:22282660
;
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:NP819502.RAPndxgtAfp0VGwnmwDi3XZL60OTLuiOEEa3ZQ3mTDM48130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:22+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" .
}