@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM
> .
@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:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_head
{
this:
np:hasAssertion
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_assertion
;
np:hasProvenance
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_provenance
;
np:hasPublicationInfo
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_assertion
a
np:Assertion
.
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_provenance
a
np:Provenance
.
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_assertion
{
miriam-gene:7132
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGN57d6edc12853c74f586f10823c49fb19
sio:SIO_000628
miriam-gene:7132
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_provenance
{
dgn-np:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_assertion
dcterms:description
"[The finding that TNFRSF1A, SCNN1B and SCNN1G are clinically relevant modulators of CF disease supports current concepts that the depletion of airway surface liquid and inadequate host inflammatory responses trigger pulmonary disease in CF.]. 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:16463024
;
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:NP669191.RAob1KWP_XgXtDZ41RmzKjBUCCM_cEEH4DpfEsk6xpWrM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}