@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA
> .
@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:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_head
{
this:
np:hasAssertion
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_assertion
;
np:hasProvenance
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_provenance
;
np:hasPublicationInfo
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_assertion
a
np:Assertion
.
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_provenance
a
np:Provenance
.
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_assertion
{
miriam-gene:729759
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN0f4c066ef924f574957b9d52af3d5837
sio:SIO_000628
miriam-gene:729759
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_provenance
{
dgn-np:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_assertion
dcterms:description
"[Polymorphisms producing small but statistically significant increases in asthma risk (OR 1.1 per allele) were identified in DPP10 and ADAM33, with the strongest evidence being for SNPs tagging the DPP10 gene.]. 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:19237393
;
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:NP575865.RAklSVZZcOrMalayzhtf5odDg17SaHdbcuUQfo2uZREOA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:47+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" .
}