@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_head
{
this:
np:hasAssertion
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_assertion
;
np:hasProvenance
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_assertion
a
np:Assertion
.
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_provenance
a
np:Provenance
.
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_assertion
{
miriam-gene:3119
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGNc046df01afa6beacf792ff80f9cdada1
sio:SIO_000628
miriam-gene:3119
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_provenance
{
dgn-np:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_assertion
dcterms:description
"[The frequency of high risk HLA alleles was significantly lower in patients with the susceptible allele at D2S137, suggesting that IDDMI3 contributes to IDDM susceptibility in subjects without high risk genotypes at IDDM1.]. 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:9498658
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1390367.RAtJWqkuheHTO6dlDpvl0K4LZ93Bz_SW5giIY_p1VQg1s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:16+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}