@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4
> .
@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:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_head
{
this:
np:hasAssertion
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_assertion
;
np:hasProvenance
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_provenance
;
np:hasPublicationInfo
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_assertion
a
np:Assertion
.
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_provenance
a
np:Provenance
.
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0376154
a
ncit:C7057
.
dgn-gda:DGNf3c14e9c14098870db2717cc4d119595
sio:SIO_000628
miriam-gene:1594
,
lld:C0376154
;
a
sio:SIO_001121
.
}
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_provenance
{
dgn-np:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_assertion
dcterms:description
"[Using conventional riboprobe in situ hybridization, VDR transcripts were readily detectable in osteoblasts within sections taken from normal bone and several actively remodelling bone tissues, namely, Paget's disease, renal hyperparathyroidism, and healing fracture callus.]. 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:8726384
;
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:NP311798.RAdBK96WnpLhTK6fKQKAfG1nyhobA9cMQXX4AkrIAHKo4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}