@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA
> .
@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:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_head
{
this:
np:hasAssertion
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion
;
np:hasProvenance
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion
a
np:Assertion
.
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance
a
np:Provenance
.
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C0153381
a
ncit:C7057
.
dgn-gda:DGN22d1c14ff6e25ecf863b5bea6a40e003
sio:SIO_000628
miriam-gene:3565
,
lld:C0153381
;
a
sio:SIO_001121
.
}
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_provenance
{
dgn-np:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_assertion
dcterms:description
"[Taken together, our results indicated that IL-4 rs2243250 polymorphism was associated with decreased oral cancer risk in both the homozygote contrasts and the dominant genetic model, as well as increased renal cell cancer risk in both the homozygote contrasts and the recessive genetic model.]. 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:23572437
;
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:NP219674.RAFkkO0iCa9k7ThxF6Xmv8Ep2tg10CpZYXnSnm3Vu6eAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}