@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE
> .
@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/v3.0.0/void/
> .
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_head
{
this:
np:hasAssertion
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion
;
np:hasProvenance
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance
;
np:hasPublicationInfo
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion
a
np:Assertion
.
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance
a
np:Provenance
.
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0013336
a
ncit:C7057
.
dgn-gda:DGNcf4cb7c3f8a77413c96f733c5318596c
sio:SIO_000628
miriam-gene:2688
,
lld:C0013336
;
a
sio:SIO_001121
.
}
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_provenance
{
dgn-np:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_assertion
dcterms:description
"[These results indicate that GH deficiency may contribute to short stature in children with Bartter syndrome, and rhGH therapy would be an excellent adjunctive treatment for short children with this syndrome whose condition is resistant to conventional therapies in terms of growth.]. 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:22707176
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP423836.RAF1x8OX5SJPZH7y6fdW_BJK6-M35p55lgXYgvSMovEwE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:46+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: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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}