@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo
> .
@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:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_head
{
this:
np:hasAssertion
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_assertion
;
np:hasProvenance
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_provenance
;
np:hasPublicationInfo
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_assertion
a
np:Assertion
.
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_provenance
a
np:Provenance
.
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_assertion
{
miriam-gene:79577
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN03367a021dba025da11655d5327f23e4
sio:SIO_000628
miriam-gene:79577
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_provenance
{
dgn-np:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_assertion
dcterms:description
"[HRPT2 and parafibromin studies improved the diagnostic accuracy in two patients with primary hyperparathyroidism (PHPT) referred to us after surgery, in whom the clinical data were at variance with the pathological diagnosis of adenoma and carcinoma, respectively.]. 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:19092296
;
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:NP455692.RAQkF89rb2vkNffu21n1-aZmq0BnNezV4f05V5BL5RAmo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}