@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc
> .
@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:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_head
{
this:
np:hasAssertion
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_assertion
;
np:hasProvenance
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_assertion
a
np:Assertion
.
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_provenance
a
np:Provenance
.
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_assertion
{
miriam-gene:3258
a
ncit:C16612
.
lld:C0342637
a
ncit:C7057
.
dgn-gda:DGN1e7d6b4ad778c9d3a4bd3c1bb4867b04
sio:SIO_000628
miriam-gene:3258
,
lld:C0342637
;
a
sio:SIO_001121
.
}
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_provenance
{
dgn-np:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_assertion
dcterms:description
"[An additional adult member (who previously underwent parathyroidectomy for neonatal severe primary hyperparathyroidism) showed an abnormality in renal clearance of calcium and sodium characteristic of combined familial hypocalciuric hypercalcemia and surgical hypoparathyroidism.]. 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:3966479
;
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:NP924179.RAsZaNXpB3bHkO0IKsC58aK9mwpvMmXLXEc9JA_x43MUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}