@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc
> .
@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:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_head
{
this:
np:hasAssertion
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_assertion
;
np:hasProvenance
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_assertion
a
np:Assertion
.
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_provenance
a
np:Provenance
.
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN5abe9f14a49ed4f87143230ead2b2815
sio:SIO_000628
miriam-gene:3126
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_provenance
{
dgn-np:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_assertion
dcterms:description
"[The extremely high frequency of HLA-DR3, DR4 heterozygotes among diabetic patients and the genetic heterogeneity in B8, DR3 positive patients on the one hand and B15, DR4 positive diabetics on the other with regard to various clinical, epidemiological and immunological parameters, point to the existence of at least two different diabetes susceptibility genes.]. 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:6333238
;
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:NP187869.RA2PeMzt-0M77uQtha8fEkrFrQ0VxJKMJ7U_zkSMjpxQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}