@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto
> .
@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:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_head
{
this:
np:hasAssertion
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_assertion
;
np:hasProvenance
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_provenance
;
np:hasPublicationInfo
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_assertion
a
np:Assertion
.
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_provenance
a
np:Provenance
.
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN83e06ccb93c80fad0507671df9efa4b5
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001122
.
}
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_provenance
{
dgn-np:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_assertion
dcterms:description
"[ABCC7 is the cystic fibrosis transmembrane conductance regulator (CFTR), and we discuss the highly prevalent CFTR mutation (F508del CFTR) in terms of the uncertainties surrounding the molecular basis of cystic fibrosis that cloud approaches to corrective therapy.]. 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:21607646
;
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:NP896436.RAUjekwYni6yujxPOQNTvVUmuRKeeEuFBjj9faE2aTKto130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:30+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" .
}