@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk
> .
@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:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_head
{
this:
np:hasAssertion
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_assertion
;
np:hasProvenance
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_assertion
a
np:Assertion
.
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_provenance
a
np:Provenance
.
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C3494506
a
ncit:C7057
.
dgn-gda:DGN2748e9576401668af67a7393ab2bc95f
sio:SIO_000628
miriam-gene:5741
,
lld:C3494506
;
a
sio:SIO_001121
.
}
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_provenance
{
dgn-np:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_assertion
dcterms:description
"[Although PPHP does not have the biochemical features of hypocalcemia and elevated parathyroid hormone levels as seen in pseudohypoparathyroidism, it seems from this case to share the potential for multiple endocrine neoplasia seen in a number of metabolic disorders in which pheochromocytoma may be a prominent manifestation.]. 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:6870447
;
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:NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}