@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o
> .
@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:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_head
{
this:
np:hasAssertion
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_assertion
;
np:hasProvenance
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_provenance
;
np:hasPublicationInfo
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_assertion
a
np:Assertion
.
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_provenance
a
np:Provenance
.
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_assertion
{
miriam-gene:79577
a
ncit:C16612
.
lld:C0262587
a
ncit:C7057
.
dgn-gda:DGN32a4ef733599e7acd0e7459e727553bf
sio:SIO_000628
miriam-gene:79577
,
lld:C0262587
;
a
sio:SIO_001121
.
}
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_provenance
{
dgn-np:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_assertion
dcterms:description
"[Our observations encourage additional study of the diagnostic potential of HRPT2 in parathyroid neoplasia and support the view that HRPT2 inactivation is not an important participant in the pathogenesis of typical parathyroid adenomas.]. 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:15956079
;
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:NP485579.RAhyuaoX1liRUS4QrrHIBxlHWxInQDM33-dghuY-YGG1o130_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" .
}