@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E
> .
@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:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_head
{
this:
np:hasAssertion
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion
;
np:hasProvenance
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance
;
np:hasPublicationInfo
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion
a
np:Assertion
.
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance
a
np:Provenance
.
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNd71c8c12f9f7ee897dcc2efe46362b31
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance
{
dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion
dcterms:description
"[Mutations of CFTR gene are responsible for cystic fibrosis (CF) and other clinical conditions such as congenital absence of the vas deferens (CAVD), chronic pancreatitis (IP), and idiopathic disseminated bronchiectasis (DBE) classified as CFTR-related disorders.]. 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:16379540
;
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:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:44+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" .
}