@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc
> .
@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:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_head
{
this:
np:hasAssertion
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion
;
np:hasProvenance
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion
a
np:Assertion
.
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance
a
np:Provenance
.
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0006277
a
ncit:C7057
.
dgn-gda:DGN3587b0c9b892507f57f2825d9a94c047
sio:SIO_000628
miriam-gene:1080
,
lld:C0006277
;
a
sio:SIO_001121
.
}
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance
{
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion
dcterms:description
"[It serves both to alert clinicians to consider CFTR-related disease in both young and elderly patients with persistent neutrophilic bronchitis, and to highlight the potential utility of future genetic testing for CFTR abnormalities in patients with asthma and recurrent bronchitis or pansinusitis, and the role of nebulized hypertonic saline as a therapeutic option in these patients.]. 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:22332135
;
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:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}