@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ
> .
@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:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_head
{
this:
np:hasAssertion
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_assertion
;
np:hasProvenance
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_assertion
a
np:Assertion
.
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_provenance
a
np:Provenance
.
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGN0f6bd535b9478a83dffc32a1f67fe275
sio:SIO_000628
miriam-gene:3630
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_provenance
{
dgn-np:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_assertion
dcterms:description
"[This mutation seemed to be maternally transmitted in the family, and the onset of diabetes was occurring earlier and the insulin secretory capacity was declining from generation to generation, so that these findings suggest that the point mutation at np 3316 is associated with various phenotypes of diabetes.]. 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:10395242
;
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:NP256722.RAmzzw3zEuWs5X9trS-nRvfwxOKC-_AOtUqrka3FruRPQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:42+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" .
}