@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4
> .
@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:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_head
{
this:
np:hasAssertion
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion
;
np:hasProvenance
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance
;
np:hasPublicationInfo
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion
a
np:Assertion
.
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance
a
np:Provenance
.
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN15bb668abc376754b9f7184e21117fc7
sio:SIO_000628
miriam-gene:5741
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_provenance
{
dgn-np:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_assertion
dcterms:description
"[We suggest that sustained stimulation of PTH receptors present in brain, muscle, and hematopoietic cells have to be considered as one independent, important cause of molecular disease in PHPT leading to profound alterations in gene expression that may help explain symptoms like muscle fatigue, cardiovascular pathology, and precipitation of psychiatric illness.]. 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:17227961
;
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:NP874138.RAKsQojBOgnXBM26_dXFvySGkYzVg2r22FvawupcK4G_4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:54+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" .
}