@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ
> .
@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:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_head
{
this:
np:hasAssertion
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion
;
np:hasProvenance
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion
a
np:Assertion
.
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance
a
np:Provenance
.
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN48cd4bc39b62db90f19cffe716a29649
sio:SIO_000628
miriam-gene:3630
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_provenance
{
dgn-np:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_assertion
dcterms:description
"[Monogenic forms of T2DM with profound defect in insulin secretion include subtypes of maturity onset diabetes of the young (MODY), maternally inherited diabetes with deafness (MIDD) caused by mitochondrial mutations, and rare cases resulting from insulin gene mutations.]. 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:15955369
;
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:NP677425.RA3SyDdTABctAjEVQZvLtN2arJ3Ibgih5NtMJcE0tFSVQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}