@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8
> .
@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:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_head
{
this:
np:hasAssertion
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_assertion
;
np:hasProvenance
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_provenance
;
np:hasPublicationInfo
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_assertion
a
np:Assertion
.
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_provenance
a
np:Provenance
.
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_assertion
{
miriam-gene:158
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGNac592bad657c83ff9084a1a398d9fbb5
sio:SIO_000628
miriam-gene:158
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_provenance
{
dgn-np:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_assertion
dcterms:description
"[Several mechanisms have been proposed to explain lung disease in CF, including abnormal airway surface liquid (ASL) properties, defective airway submucosal gland function, altered inflammatory response, defective organellar acidification, loss of CFTR regulation of plasma membrane ion transporters, and others.]. 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:12475759
;
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:NP489616.RA9TCho1SdotgSNZjtw4XljYs6QJdy3jHyc83wnyRdSU8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}