@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8
> .
@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:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_head
{
this:
np:hasAssertion
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_assertion
;
np:hasProvenance
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_provenance
;
np:hasPublicationInfo
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_assertion
a
np:Assertion
.
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_provenance
a
np:Provenance
.
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0011847
a
ncit:C7057
.
dgn-gda:DGNe7c20504c77d45598f94987b27c81e0b
sio:SIO_000628
miriam-gene:2688
,
lld:C0011847
;
a
sio:SIO_001121
.
}
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_provenance
{
dgn-np:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_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:NP574017.RAzkwhFaxjHjb8csBKzXbaPiBoUV6H6fpX0NQPLRGUQo8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}