@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0
> .
@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:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_head
{
this:
np:hasAssertion
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion
;
np:hasProvenance
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion
a
np:Assertion
.
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance
a
np:Provenance
.
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN0bc94c0566f4f64e4686a01174b37473
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance
{
dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion
dcterms:description
"[Cystic fibrosis (CF) is a common, fatal hereditary disease resulting from mutations of the human cystic fibrosis transmembrane conductance regulator (CFTR) gene in which epithelial cells throughout the body manifest altered regulation of apical membrane chloride secretion.]. 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:7948135
;
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:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:48+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" .
}