@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww
> .
@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:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_head
{
this:
np:hasAssertion
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_assertion
;
np:hasProvenance
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_provenance
;
np:hasPublicationInfo
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_assertion
a
np:Assertion
.
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_provenance
a
np:Provenance
.
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_assertion
{
miriam-gene:6928
a
ncit:C16612
.
lld:C0268800
a
ncit:C7057
.
dgn-gda:DGN96eca8d45e80dbc175b17a2f63942cf6
sio:SIO_000628
miriam-gene:6928
,
lld:C0268800
;
a
sio:SIO_001121
.
}
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_provenance
{
dgn-np:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_assertion
dcterms:description
"[Between 2002 and 2009, we screened 50 of 150 patients referred for kidney and pancreas transplantation to the Kremlin-Bicêtre center for HNF1B and HNF1A mutations if one or more of the following criteria was present (i) an atypical history of diabetes (ii) diabetes with at least one affected parent or two affected relatives, (iii) an absence of auto-antibodies at diagnosis (iv) a persistent secretion of fasting C peptide (v) a personal or a family history of renal cysts or dysplasia.]. 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:22432796
;
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:NP779711.RALDSQf1-q-EYa37YSMyccJmmy1FDvX_6EjG0sQkZ8-ww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}