@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo
> .
@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:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_head
{
this:
np:hasAssertion
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_assertion
;
np:hasProvenance
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_provenance
;
np:hasPublicationInfo
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_assertion
a
np:Assertion
.
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_provenance
a
np:Provenance
.
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C0008312
a
ncit:C7057
.
dgn-gda:DGN862382d2adf98befa1262608f3ab6ba6
sio:SIO_000628
miriam-gene:1594
,
lld:C0008312
;
a
sio:SIO_001121
.
}
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_provenance
{
dgn-np:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_assertion
dcterms:description
"[In conclusion, the COLIA1 but not VDR polymorphism is a genetic marker of peak bone mass in patients with PBC, although the severity of cholestasis is the main factor for osteoporosis since it is associated with the rate of bone loss.]. 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:11230734
;
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:NP469471.RAB454TMi3ErhKlA1ZJoBzLStMfbZYoH2FWrS2p9pymGo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}