@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o
> .
@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 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:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_head
{
this:
np:hasAssertion
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion
;
np:hasProvenance
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance
;
np:hasPublicationInfo
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion
a
np:Assertion
.
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance
a
np:Provenance
.
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion
{
miriam-gene:767
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGNd0c569fdee10f53675023583da0d9dc1
sio:SIO_000628
miriam-gene:767
,
lld:C0029456
;
a
sio:SIO_001122
.
}
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_provenance
{
dgn-np:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_assertion
dct:description
"[Here, we investigated single nucleotide polymorphisms (SNPs) in carbonic anhydrase genes that are expressed in bone tissues, i.e., CA8 and CA10, for possible association with femoral and lumbar BMD among 337 Japanese women with osteoporosis participated in BioBank Japan project.]. 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:19172221
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP79484.RA5AfDN8ADz18Bfy-RJtxW-7T7UaRAPBBt46UM5fvVh_o130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}