@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o
> .
@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:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_head
{
this:
np:hasAssertion
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_assertion
;
np:hasProvenance
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_provenance
;
np:hasPublicationInfo
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_assertion
a
np:Assertion
.
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_provenance
a
np:Provenance
.
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN6b83c75f9b398d3cba7d5ffc49d06c2f
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_provenance
{
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_assertion
dcterms:description
"[The CFTR mutations in cystic fibrosis (CF) lead to ion transport anomalities which predispose to chronic infection and inflammation of CF airways as the major determinants for morbidity and mortality in CF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:16463024
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP11686.RADAsTAhuhgyab9lZxeg1srcMpPEBxYdyMRb8hq8MiI4o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:03+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" .
}