@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U
> .
@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 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:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_head
{
this:
np:hasAssertion
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion
;
np:hasProvenance
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance
;
np:hasPublicationInfo
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion
a
np:Assertion
.
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance
a
np:Provenance
.
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNadbd3185a779e38b7eeefab16f0282d1
sio:SIO_000628
miriam-gene:1080
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance
{
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion
dct:description
"[In order to investigate the incidence of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and unclassified variants in chronic pulmonary disease in children and adults, we studied 20 patients with asthma, 19 with disseminated bronchiectasis (DB) of unknown aetiology, and 12 patients with chronic obstructive pulmonary disease (COPD), and compared the results to 52 subjects from the general Greek population.]. 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:11354633
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}