@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_head
{
this:
np:hasAssertion
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion
;
np:hasProvenance
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion
a
np:Assertion
.
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance
a
np:Provenance
.
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNe5784daa7a8ec260c50ee4870e341af7
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance
{
dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion
dcterms:description
"[Cystic Fibrosis (CF) is an autosomal recessive disorder due to mutations in the CF transmembrane conductance regulator (CFTR) gene that lead to defective ion transport in the conducting pulmonary airways and exocrine glands.]. 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:18600482
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:53+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}