@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo
> .
@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:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_head
{
this:
np:hasAssertion
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_assertion
;
np:hasProvenance
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_provenance
;
np:hasPublicationInfo
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_assertion
a
np:Assertion
.
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_provenance
a
np:Provenance
.
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN5cdf03ba5dca53df79912433d207bc75
sio:SIO_000628
miriam-gene:1756
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_provenance
{
dgn-np:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_assertion
dcterms:description
"[Our present results suggest that the rs2073438 polymorphism of ALOX12 contributes to the variation of obesity phenotypes in young Chinese men, although we failed to replicate the association with the peak BMD variation in this sample.]. 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:20697415
;
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:NP570449.RAe1uDMcxmbaMmqdatcdN7VEvvLQ5TJKlgp59cISekCYo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}