@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion
a
np:Assertion
.
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_provenance
a
np:Provenance
.
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNd30c3f3f8b04e5990659ad664e22d074
sio:SIO_000628
miriam-gene:6774
,
lld:C0004096
;
a
sio:SIO_001121
.
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dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_provenance
{
dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_assertion
dcterms:description
"[Our results indicate that genetic variants in STAT3, independent of asthma treatment, are determinants of FEV1 in both adults and children with asthma, and suggest that STAT3 may participate in inflammatory pathways that have an impact on level of lung function.]. 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:15935090
;
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 .
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dgn-np:NP241634.RASPBlMfbYruiKpDaWvbQhohh0kzSc-W8LWKNoLYaIh38130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:15+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
<
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> , <
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" .
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