@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w
> .
@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:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_head
{
this:
np:hasAssertion
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_assertion
;
np:hasProvenance
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_provenance
;
np:hasPublicationInfo
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_assertion
a
np:Assertion
.
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_provenance
a
np:Provenance
.
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_assertion
{
miriam-gene:126014
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN86ea182f15c9e07f58ee26c0da89848f
sio:SIO_000628
miriam-gene:126014
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_provenance
{
dgn-np:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_assertion
dcterms:description
"[In an effort to identify genetic polymorphisms in potential candidate genes for osteoporosis, 10 variants were identified in the OSCAR gene using direct DNA sequencing, and 560 postmenopausal women were genotyped at five SNP loci, using the TaqMan method.]. 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:16007331
;
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:NP934371.RAhh8kniJqhDDyJu6Chv5ElqoocG9szHVupvJ_C4GtB6w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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" .
}