@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY
> .
@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:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_head
{
this:
np:hasAssertion
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_assertion
;
np:hasProvenance
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_assertion
a
np:Assertion
.
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_provenance
a
np:Provenance
.
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0004031
a
ncit:C7057
.
dgn-gda:DGN5f4b2219951a00bd00bf9351274333c6
sio:SIO_000628
miriam-gene:1080
,
lld:C0004031
;
a
sio:SIO_001121
.
}
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_provenance
{
dgn-np:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_assertion
dcterms:description
"[To test this possibility, the entire coding region of the cystic fibrosis transmembrane regulator (CFTR) gene was analyzed in 11 individuals who met strict criteria for the diagnosis of ABPA and had normal sweat electrolytes (< or = 40 mmol/liter).]. 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:8659542
;
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:NP697795.RA2T6rCPnQ_zD9bfJfPdE90Yvq95-bfATuFzRsnB8zkHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}