@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw
> .
@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:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_head
{
this:
np:hasAssertion
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion
;
np:hasProvenance
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion
a
np:Assertion
.
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance
a
np:Provenance
.
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0151317
a
ncit:C7057
.
dgn-gda:DGN647fcecd8046dacca3b76dab607378c2
sio:SIO_000628
miriam-gene:1080
,
lld:C0151317
;
a
sio:SIO_001121
.
}
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_provenance
{
dgn-np:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_assertion
dcterms:description
"[The CFTR mutations in cystic fibrosis (CF) lead to ion transport anomalities which predispose to chronic infection and inflammation of CF airways as the major determinants for morbidity and mortality in CF.]. 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:16463024
;
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:NP874623.RAC2S5av6PXDT5dftUTDd0dkV-1IOC3NvevUFNDWQjAqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}