@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs
> .
@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:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_head
{
this:
np:hasAssertion
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion
;
np:hasProvenance
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance
;
np:hasPublicationInfo
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion
a
np:Assertion
.
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance
a
np:Provenance
.
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion
{
miriam-gene:138428
a
ncit:C16612
.
lld:C0342637
a
ncit:C7057
.
dgn-gda:DGNd8f60a3db2c76fec45169e4ba02dcb0e
sio:SIO_000628
miriam-gene:138428
,
lld:C0342637
;
a
sio:SIO_001121
.
}
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_provenance
{
dgn-np:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_assertion
dcterms:description
"[Therefore, a biochemical phenotype of PTH-dependent hypercalcemia resembling that caused by heterozygous inactivating mutations of the CaR in familial hypocalciuric hypercalcemia can be observed in patients with antibodies to the CaR's extracellular domain that stimulate PTH release, probably by inhibiting activation of the CaR by Ca(2+)(o).]. 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:12519831
;
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:NP629490.RARtxvRGq1iYI6WjHOHvZQfpHTNwNyl-3JAHxoOaDoYVs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:20+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" .
}