@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_head
{
this:
np:hasAssertion
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_assertion
;
np:hasProvenance
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_assertion
a
np:Assertion
.
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_provenance
a
np:Provenance
.
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN6b81e3affcc68d9dd8f64469bcac0d48
sio:SIO_000628
miriam-gene:183
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_provenance
{
dgn-np:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_assertion
dcterms:description
"[In-depth analysis of this haplotype with other methods of Wald statistics and Akaike information criterion confirmed that carriers of each unit of this haplotype AGT increases the risk of osteoporosis by a factor of 2.80±0.34 (β±SE) which manifests (P=0.1 × 10⁻⁶) in its recessive mode of inheritance.]. 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:23975234
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP229267.RAx9k5XbR76DP8A5rUKzoM8By5VNvWIxSYO6VzssS7bUQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:50+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}