@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_head
{
this:
np:hasAssertion
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_assertion
;
np:hasProvenance
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_assertion
a
np:Assertion
.
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_provenance
a
np:Provenance
.
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_assertion
{
miriam-gene:4842
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNea1e48264c43bcaadaebf4aa4ee4bb02
sio:SIO_000628
miriam-gene:4842
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_provenance
{
dgn-np:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_assertion
dcterms:description
"[The aim of this study was to investigate whether the number of AAT repeats in intron 20 of the NOS1 gene, recently associated with variations in FENO in adults with asthma and cystic fibrosis, was associated with the raised FENO in healthy atopic children.]. 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:12911502
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP405053.RAsve8KV2oeMPB_sr3cdEnzessPT35ms4t0I64DPjUodQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:48+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
}