@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0
> .
@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:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_head
{
this:
np:hasAssertion
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_assertion
;
np:hasProvenance
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_assertion
a
np:Assertion
.
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_provenance
a
np:Provenance
.
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0037176
a
ncit:C7057
.
dgn-gda:DGN462e6753865cf8c4034038b9979f0957
sio:SIO_000628
miriam-gene:3630
,
lld:C0037176
;
a
sio:SIO_001121
.
}
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_provenance
{
dgn-np:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_assertion
dcterms:description
"[Only a minority of cases of type 2 diabetes are caused by single gene defects such as maturity onset diabetes of the young (MODY), syndrome of insulin resistance (insulin receptor defect) and maternally inherited diabetes and deafness (mitochondrial gene defect).]. 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:14748467
;
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:NP700647.RAoRZ5Bcb_vRL-1ChIsO7Rjfwl5mQxAh6geQSeL4DuDx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}