@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA
> .
@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:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_head
{
this:
np:hasAssertion
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_assertion
;
np:hasProvenance
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_provenance
;
np:hasPublicationInfo
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_assertion
a
np:Assertion
.
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_provenance
a
np:Provenance
.
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_assertion
{
miriam-gene:1040
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNa24480a9a2a49bbee62015d5d384b607
sio:SIO_000628
miriam-gene:1040
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_provenance
{
dgn-np:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_assertion
dcterms:description
"[Cultured peripheral blood leukocytes (PBL) from individuals homozygous or heterozygous for the defective gene causing the inherited disease cystic fibrosis (CF) secrete three different ciliary dyskinesia substances (CDS), which can be detected by their activity in vitro in a rabbit mucociliary bioassay.]. 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:7430342
;
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:NP251444.RAKwT_PIeJcwE8Hk1_tUnsNH0eJBJheG4H6-IgLUDKhMA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}