@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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{
this:
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dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion
a
np:Assertion
.
dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_provenance
a
np:Provenance
.
dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3459
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN22622b41a1c19c2b4655fc1f9da52e9a
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miriam-gene:3459
,
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;
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.
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dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_provenance
{
dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_assertion
dcterms:description
"[We have used a stepwise approach consisting of initial interrogation, confirmation and fine mapping to analyze STAT3, IL1B and IFNGR1 as modifiers of cystic fibrosis disease building upon the data and sample collection of the European Cystic Fibrosis Twin and Sibling Study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:21731057
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP648161.RARbexFXA4MypqQYbnoHeq_knmW3yC38369_ylt4xt-cs130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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