@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8
> .
@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:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_head
{
this:
np:hasAssertion
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_assertion
a
np:Assertion
.
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_provenance
a
np:Provenance
.
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0020503
a
ncit:C7057
.
dgn-gda:DGNf271452d7dfd34a89db56e0aad6d0000
sio:SIO_000628
miriam-gene:4221
,
lld:C0020503
;
a
sio:SIO_001121
.
}
dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_provenance
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dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_assertion
dcterms:description
"[In this study we examined the expression of menin in parathyroid tumors from primary hyperparathyroidism (PHP), secondary hyperparathyroidism (SHP), and MEN1 and thyroid tumors including Basedow's disease, thyroid cancer, and adrenocortical tumors.]. 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:10902816
;
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 .
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dgn-np:NP485077.RAcaopqxsLXPl69jIF9RTddVH8cbRWay2ztmwrtXn4Ap8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}