@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4
> .
@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:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_head
{
this:
np:hasAssertion
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_assertion
;
np:hasProvenance
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_provenance
;
np:hasPublicationInfo
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_assertion
a
np:Assertion
.
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_provenance
a
np:Provenance
.
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0020438
a
ncit:C7057
.
dgn-gda:DGN556e95ad155921c37bf5f5db6de0ec44
sio:SIO_000628
miriam-gene:5741
,
lld:C0020438
;
a
sio:SIO_001121
.
}
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_provenance
{
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_assertion
dcterms:description
"[Episodes were generally mild, and nearly all cases resolved spontaneously or with discontinuation of calcium and vitamin D. The algorithms used to address hypercalcemia and hypercalciuria in the PaTH trial proved effective in safely resolving clinical episodes of increased urinary or serum calcium and might therefore be helpful to clinicians caring for patients on PTH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:17164314
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP27838.RAcUGM8pI2DvoH4o_mINmyWIeqEpCiARar7M-aAOMbIS4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:11+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: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" .
}