@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A
> .
@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:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_head
{
this:
np:hasAssertion
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_assertion
;
np:hasProvenance
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_provenance
;
np:hasPublicationInfo
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_assertion
a
np:Assertion
.
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_provenance
a
np:Provenance
.
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0006663
a
ncit:C7057
.
dgn-gda:DGN2def6025807f1268dd7a16449dff884a
sio:SIO_000628
miriam-gene:5741
,
lld:C0006663
;
a
sio:SIO_001121
.
}
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_provenance
{
dgn-np:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_assertion
dcterms:description
"[In three siblings with autosomal recessive idiopathic strio-pallido-dentate calcinosis (SPDC) and in three other siblings with Cockayne's syndrome (CS) studies on plasma values of calcium and phosphate, intestinal calcium absorption, radiograms of the hands and studies on the influence of parathyroid hormone (PTH) on the renal threshold for phosphate revealed no abnormalities.]. 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:6315288
;
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:NP847511.RANp73bHk-r2UykY0yzOC4eSUTUwVYsAhEKttJmeM317A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}