@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE
> .
@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:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_head
{
this:
np:hasAssertion
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion
;
np:hasProvenance
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion
a
np:Assertion
.
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance
a
np:Provenance
.
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion
{
miriam-gene:59271
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNadb55b64c815ef32e1e41e63459c47e0
sio:SIO_000628
miriam-gene:59271
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_provenance
{
dgn-np:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_assertion
dcterms:description
"[The frequency of the whole haplotype Cw5, B18, BfF1, DR3 and of its segment BfF1, DR3, and the strength of the gametic associations between these alleles were much higher in IDD patients than in non-diabetic controls, irrespective of the age of onset of their diabetes.]. 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:6607851
;
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:NP604479.RAOknxrmMvb_fLxqPjrQobF7u7MXd1Gldyh2CuXxuVrNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}