@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_head
{
this:
np:hasAssertion
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_assertion
;
np:hasProvenance
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_provenance
;
np:hasPublicationInfo
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_assertion
a
np:Assertion
.
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_provenance
a
np:Provenance
.
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_assertion
{
miriam-gene:4638
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN91f333c87673bc307ed694ed47a3d346
sio:SIO_000628
miriam-gene:4638
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_provenance
{
dgn-np:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_assertion
dcterms:description
"[These data suggest that CTTN gene variation may contribute to severe asthma and that the combined effects of CTTN and MYLK risk polymorphisms may further increase susceptibility to severe asthma in African Americans harboring both genetic variants.]. 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:18521921
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP85202.RAwVecTaQ6n-NOKKx1_gSJ8NxTo-k17oOrVISLgmdzNb8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:26+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}