@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg
> .
@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:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_head
{
this:
np:hasAssertion
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_assertion
;
np:hasProvenance
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_provenance
;
np:hasPublicationInfo
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_assertion
a
np:Assertion
.
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_provenance
a
np:Provenance
.
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN5b41fe4dd40bdded5fe78bf60a694d8e
sio:SIO_000628
miriam-gene:1861
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_provenance
{
dgn-np:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_assertion
dcterms:description
"[This suggests that if all alleles are truly identical for the major A1, B8, DR3 haplotype (between A1 and DR3), with different alleles on nonconserved haplotypes without differential diabetes risk, then in this region of the genome DR3-DQ2 may be the primary polymorphisms of common haplotypes contributing to diabetes risk.]. 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:15919812
;
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:NP847968.RAULvof7ffOpt_EJSF-4TVt23lcvO8iOExHtLVXx73jXg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}