@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI
> .
@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:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_head
{
this:
np:hasAssertion
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion
;
np:hasProvenance
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion
a
np:Assertion
.
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance
a
np:Provenance
.
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN29b69132d22aaaccc62743e96d332c54
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance
{
dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion
dcterms:description
"[Cystic fibrosis, the most common lethal genetic disease affecting young people in North America, is caused by failure of the chloride ion channel known as CFTR (cystic fibrosis transmembrane conductance regulator).]. 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:25367045
;
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:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:05+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" .
}