@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040
> .
@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:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_head
{
this:
np:hasAssertion
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_assertion
;
np:hasProvenance
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_provenance
;
np:hasPublicationInfo
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_assertion
a
np:Assertion
.
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_provenance
a
np:Provenance
.
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_assertion
{
miriam-gene:1934
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN49074c03d84a4cc3b810a4a825dd4d5d
sio:SIO_000628
miriam-gene:1934
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_provenance
{
dgn-np:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_assertion
dcterms:description
"[The DQ beta sequence from the DR4 haplotype was identical to the predominant DR4 allele (DQ beta 3.2) but differed at four amino acid residues from the other major DR4 DQ beta sequence (DQ beta 3.1) found rarely among IDDM patients.]. 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:3372263
;
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:NP447695.RAiTiX_-Wv8FAC8hQtWxKKBP1N5-1IxhdXQxwTMUfr040130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}