@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM
> .
@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:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_head
{
this:
np:hasAssertion
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion
;
np:hasProvenance
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion
a
np:Assertion
.
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance
a
np:Provenance
.
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion
{
miriam-gene:138428
a
ncit:C16612
.
lld:C0020437
a
ncit:C7057
.
dgn-gda:DGNea8549c822ea2342c4f192a11288791a
sio:SIO_000628
miriam-gene:138428
,
lld:C0020437
;
a
sio:SIO_001121
.
}
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_provenance
{
dgn-np:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_assertion
dcterms:description
"[In a case of neonatal severe hyperparathyroidism characterized by moderately severe hypercalcemia and very high PTH levels, coupled with evidence of hyperparathyroidism and effects on brain development not previously demonstrated, we detected point mutations on separate alleles of the CaR, resulting in premature stop codon substitutions at G94 and R648.]. 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:15292296
;
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:NP454558.RAkMuCTK3LAEynXBvCsjSqLQSOnTqezw7F_JIbdXInbMM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:11+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" .
}