@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg
> .
@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:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_head
{
this:
np:hasAssertion
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_assertion
;
np:hasProvenance
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_assertion
a
np:Assertion
.
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_provenance
a
np:Provenance
.
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_assertion
{
miriam-gene:1594
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN6ce3b4676fc10134b58ef4998a797013
sio:SIO_000628
miriam-gene:1594
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_provenance
{
dgn-np:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_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:NP272188.RAoY5mn2MhmymPZ0VI4Vf4H2O8rln2_MGOTO95rHMDOHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}