@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4
> .
@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:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_head
{
this:
np:hasAssertion
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_assertion
;
np:hasProvenance
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_provenance
;
np:hasPublicationInfo
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_assertion
a
np:Assertion
.
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_provenance
a
np:Provenance
.
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0005940
a
ncit:C7057
.
dgn-gda:DGN85cd7977429a97109433435f5ed3cda2
sio:SIO_000628
miriam-gene:1756
,
lld:C0005940
;
a
sio:SIO_001121
.
}
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_provenance
{
dgn-np:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_assertion
dcterms:description
"[This study shows for the first time that the polymorphisms polyAla and Pro198Leu of the GPX1 gene, individually and in combination, are associated with BMD and therefore may be useful as genetic markers for bone disease.]. 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:21045266
;
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:NP931034.RA9uETKCRjizukorCI-cbMxv2KAy_If1x3EJu9AVMLZO4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}