@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws
> .
@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:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_head
{
this:
np:hasAssertion
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_assertion
;
np:hasProvenance
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_provenance
;
np:hasPublicationInfo
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_assertion
a
np:Assertion
.
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_provenance
a
np:Provenance
.
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_assertion
{
miriam-gene:3258
a
ncit:C16612
.
lld:C0221002
a
ncit:C7057
.
dgn-gda:DGNcccfb31d8882038d1adbbed53678eed5
sio:SIO_000628
miriam-gene:3258
,
lld:C0221002
;
a
sio:SIO_001121
.
}
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_provenance
{
dgn-np:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_assertion
dcterms:description
"[In view of its success in avoiding the complication of repeated neck exploration for recurrent hyperparathyroidism or the creation of permanent hypoparathyroidism, we recommend this surgical approach for the rare neonate with primary hyperparathyroidism.]. 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:3522845
;
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:NP926386.RAAOhC0BQPKdBV3zGIZmyZHhMhvu4hfUNOSymRr6mVnws130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}