@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_assertion
;
np:hasProvenance
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_provenance
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np:hasPublicationInfo
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_assertion
a
np:Assertion
.
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_provenance
a
np:Provenance
.
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN4e0db57b124521274766f4d59089d980
sio:SIO_000628
miriam-gene:3565
,
lld:C0024117
;
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sio:SIO_001121
.
}
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_provenance
{
dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_assertion
dcterms:description
"[Genetic variants of the two adjacent genes, IL13 and IL4 have frequently been reported as being associated with susceptibility to atopy and asthma, both in adults and children, and some studies also suggest association with lung function and chronic obstructive pulmonary disease.]. 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:19254294
;
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 .
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dgn-np:NP693932.RAG3-h36zqpAphyraC8T5FjfdZ22MyrBve_YzU5RoZONM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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
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pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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
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