@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs
> .
@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:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_head
{
this:
np:hasAssertion
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_assertion
;
np:hasProvenance
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_assertion
a
np:Assertion
.
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_provenance
a
np:Provenance
.
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C0035235
a
ncit:C7057
.
dgn-gda:DGN315e258140dc77ec4186b977392bb85f
sio:SIO_000628
miriam-gene:3565
,
lld:C0035235
;
a
sio:SIO_001121
.
}
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_provenance
{
dgn-np:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_assertion
dcterms:description
"[To investigate the genetic basis for RSV disease severity, linked variants of 3 Th2 cytokine genes, IL4, IL13, and IL5 (which are clustered on chromosome 5q31.1) were characterized in 105 children who were hospitalized with severe RSV infection and 315 Korean control subjects in a pilot study.]. 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:12402189
;
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:NP676100.RA8MuDPJPQtZm6F4X2Eu7tH7AoNKZuTEg_4ghAK9UEQcs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}