@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0
> .
@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:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_head
{
this:
np:hasAssertion
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_assertion
;
np:hasProvenance
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_provenance
;
np:hasPublicationInfo
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_assertion
a
np:Assertion
.
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_provenance
a
np:Provenance
.
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_assertion
{
miriam-gene:57628
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN71bf39be51b9f01c7b06e39dd0923fb2
sio:SIO_000628
miriam-gene:57628
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_provenance
{
dgn-np:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_assertion
dcterms:description
"[Overall, the contribution of rare variants to asthma susceptibility was predominantly due to noncoding variants in sequences flanking the exons, although nonsynonymous rare variants in DPP10 and in IL12RB1 were associated with asthma in African Americans and European Americans, respectively.]. 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:22325360
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP932521.RAdMoeFeFA-fbLg3ZnKjsmQE65BjaKlaTaGLkrWqHU6h0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:09+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" .
}