@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM
> .
@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:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_head
{
this:
np:hasAssertion
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_assertion
;
np:hasProvenance
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_provenance
;
np:hasPublicationInfo
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_assertion
a
np:Assertion
.
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_provenance
a
np:Provenance
.
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_assertion
{
miriam-gene:57380
a
ncit:C16612
.
lld:C0221002
a
ncit:C7057
.
dgn-gda:DGNb5b28ad546fffe9f0dec465994beed22
sio:SIO_000628
miriam-gene:57380
,
lld:C0221002
;
a
sio:SIO_001121
.
}
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_provenance
{
dgn-np:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_assertion
dcterms:description
"[Primary hyperparathyroidism (pHPT) is characterized by excessive production of parathyroid hormone (PTH) due to parathyroid adenomas while uremic secondary HPT (sHPT) is caused by parathyroid hyperplasia in response to renal failure.]. 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:12444900
;
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:NP246673.RAQFHQSsTjxfDrbruS3Vg4UAfUmMy52gw1Bq5tPE6d4CM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}