@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc
> .
@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/v4.0.0/void/
> .
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_head
{
this:
np:hasAssertion
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion
;
np:hasProvenance
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion
a
np:Assertion
.
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance
a
np:Provenance
.
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion
{
miriam-gene:114327
a
ncit:C16612
.
lld:C0270850
a
ncit:C7057
.
dgn-gda:DGN4362b31eaf43d5fb7211566f7e6d8e57
sio:SIO_000628
miriam-gene:114327
,
lld:C0270850
;
a
sio:SIO_001121
.
}
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_provenance
{
dgn-np:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_assertion
dcterms:description
"[We also genotyped specific EFHC1 variants in IGE cases and controls from multiple ethnic backgrounds, including 17 African American IGE patients, with 24 matched controls, and 92 Caucasian JME patients with 103 matched controls.]. 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:25489633
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1246359.RArB2i7em3O1vQoTHOmrefh5p8ncgmcFnQ6hH1IH_5ZSc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:10+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}