@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg
> .
@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:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_head
{
this:
np:hasAssertion
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_assertion
;
np:hasProvenance
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_provenance
;
np:hasPublicationInfo
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_assertion
a
np:Assertion
.
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_provenance
a
np:Provenance
.
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN799559bd3fc6d83ea99fe7b32fb45ca9
sio:SIO_000628
miriam-gene:7439
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_provenance
{
dgn-np:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_assertion
dcterms:description
"[Our study identified many SNPs in the SOX6 gene associated with hip BMD even across different ethnicities, which further highlighted the importance of the SOX6 gene influencing BMD variation and provided more information to the understanding of the genetic architecture of osteoporosis.]. 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:21625884
;
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:NP160558.RAxNyi8VhnM6Ua5cXsk661NJc1taOwI0MWW_bNX93ktzg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}