@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU
> .
@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:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_head
{
this:
np:hasAssertion
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_assertion
;
np:hasProvenance
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_provenance
;
np:hasPublicationInfo
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_assertion
a
np:Assertion
.
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_provenance
a
np:Provenance
.
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_assertion
{
miriam-gene:3557
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNd4f55364782b1afe911952305a4ae2f4
sio:SIO_000628
miriam-gene:3557
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_provenance
{
dgn-np:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_assertion
dcterms:description
"[DNA samples from the German centres of the European Community Respiratory Health Survey were analysed for genetic variants in the IL1RA gene and the development of asthma, atopy and bronchial hyperreactivity.]. 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:16409203
;
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:NP446489.RAQybD8EE7GDPCM5tzy21Z88vM4mIQuQ3Tp3VghrdxzwU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}