@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI
> .
@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:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_head
{
this:
np:hasAssertion
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_assertion
;
np:hasProvenance
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_assertion
a
np:Assertion
.
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_provenance
a
np:Provenance
.
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0267963
a
ncit:C7057
.
dgn-gda:DGNa6422031d94682a6269d9ff43cef5d2b
sio:SIO_000628
miriam-gene:1080
,
lld:C0267963
;
a
sio:SIO_001121
.
}
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_provenance
{
dgn-np:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_assertion
dcterms:description
"[Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that results in abnormal viscous mucoid secretions in multiple organs and whose main clinical features are pancreatic insufficiency and chronic endobronchial infection.]. 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:18506640
;
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:NP553946.RAH1dVCv7WnHV2Wosa5_YTH2wL7yqERztUFoq6BzldbOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:34+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" .
}