@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48
> .
@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:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_head
{
this:
np:hasAssertion
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_assertion
;
np:hasProvenance
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_provenance
;
np:hasPublicationInfo
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_assertion
a
np:Assertion
.
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_provenance
a
np:Provenance
.
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_assertion
{
miriam-gene:3481
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN6dd7030fa1292b40d0d1cdbb1c9f17af
sio:SIO_000628
miriam-gene:3481
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_provenance
{
dgn-np:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_assertion
dcterms:description
"[ID- alleles are only clearly distinguished from all other alleles by an MSPI(-) variant within IGF2 downstream of the minisatellite, suggesting that the apparent role of the minisatellite in susceptibility to T1DM may be modified by neighbouring haplotype and therefore that IDDM2 could have a multi-locus aetiology.]. 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:11115836
;
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:NP698088.RAQPBYcXcLF1KZof_874TFmkvJVG8-qFiBOWLRbpRVr48130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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
<
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> , <
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" .
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"v2.1.0" .
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