@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ
> .
@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:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_head
{
this:
np:hasAssertion
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_assertion
;
np:hasProvenance
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_assertion
a
np:Assertion
.
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_provenance
a
np:Provenance
.
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_assertion
{
miriam-gene:6927
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGN4ac2045a50af0be2bef92c965dbed1e6
sio:SIO_000628
miriam-gene:6927
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_provenance
{
dgn-np:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_assertion
dcterms:description
"[The appearance of fasting hyperglycaemia following rhGH treatment in children with renal cystic hypodysplasia suggests that investigation of the HNF1 beta gene is warranted, even when familial history is negative for 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:20543213
;
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:NP260813.RAM3U411AeM6zUd7ZyH3_v6LFOeySEdofvkOlDjdQF9kQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:25+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" .
}