@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A
> .
@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#
> .
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_head
{
this:
np:hasAssertion
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_assertion
;
np:hasProvenance
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_provenance
;
np:hasPublicationInfo
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_assertion
a
np:Assertion
.
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_provenance
a
np:Provenance
.
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_assertion
{
miriam-gene:29980
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGNdefc2c013fd8a75b19636eda3a23830c
sio:SIO_000628
miriam-gene:29980
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_provenance
{
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_assertion
dcterms:description
"[HLA-A and -B typing performed on 231 IDDM individuals and 268 controls from the southeastern U.S. showed significant increases with IDDM in A2, B8, B15 and B18, and significant decreases in Aw23, B7, B14 and B17.]. 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:6411398
;
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 .
}
dgn-np:NP562263.RAGmiGoF1lQ1hL1mV8GEqULHgu8Y_F2ZU0sOmW7BGT51A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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
<
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}