@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc
> .
@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:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_head
{
this:
np:hasAssertion
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion
;
np:hasProvenance
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion
a
np:Assertion
.
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance
a
np:Provenance
.
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion
{
miriam-gene:4353
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN63e0f897e5e9d30aa0223e42d605889e
sio:SIO_000628
miriam-gene:4353
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance
{
dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion
dcterms:description
"[Cystic fibrosis is a debilitating lung disease due to mutations in the cystic fibrosis transmembrane conductance regulator protein (CFTR) and is associated with chronic infections resulting in elevated myeloperoxidase activity and generation of hypochlorous acid (HOCl).]. 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:20799947
;
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:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:04+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" .
}