@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8
> .
@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:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_head
{
this:
np:hasAssertion
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_assertion
;
np:hasProvenance
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_provenance
;
np:hasPublicationInfo
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_assertion
a
np:Assertion
.
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_provenance
a
np:Provenance
.
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_assertion
{
miriam-gene:340719
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN08f49262104eb37cd0fce7e5296cef22
sio:SIO_000628
miriam-gene:340719
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_provenance
{
dgn-np:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_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-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:NP659532.RA9nV-KQs8kgQkV1V06tCMzMA-t173ffPrFalwMmamzR8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}