@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA
> .
@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:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_head
{
this:
np:hasAssertion
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_assertion
;
np:hasProvenance
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_provenance
;
np:hasPublicationInfo
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_assertion
a
np:Assertion
.
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_provenance
a
np:Provenance
.
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0020437
a
ncit:C7057
.
dgn-gda:DGN082f8298ea683121fee09d92e8f83350
sio:SIO_000628
miriam-gene:4221
,
lld:C0020437
;
a
sio:SIO_001121
.
}
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_provenance
{
dgn-np:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_assertion
dcterms:description
"[However, the demonstration of LOH at 11q13 and MEN1 gene mutations in small parathyroid adenomas of patients with slight hypercalcemia and normal serum PTH levels suggest that altered MEN1 gene function may also be important for the development of mild sporadic pHPT.]. 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:9709976
;
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:NP872915.RAjJc_zgCjhZNU8PP1hbEdh_E8unsTz141-852KpD6AoA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}