@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE
> .
@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:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_head
{
this:
np:hasAssertion
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_assertion
;
np:hasProvenance
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_provenance
;
np:hasPublicationInfo
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_assertion
a
np:Assertion
.
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_provenance
a
np:Provenance
.
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNc456c40f86f10316b62e37d32730b662
sio:SIO_000628
miriam-gene:3630
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_provenance
{
dgn-np:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_assertion
dcterms:description
"[Functional studies showed that recessive mutations resulted in diabetes because of decreased insulin biosynthesis through distinct mechanisms, including gene deletion, lack of the translation initiation signal, and altered mRNA stability because of the disruption of a polyadenylation signal.]. 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:20133622
;
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:NP791991.RALNhTkNQwMq2tvWaUK4e1Q2HOADqZnqX_PKZF0Sd2EAE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:44+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" .
}