@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI
> .
@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:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_head
{
this:
np:hasAssertion
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_assertion
;
np:hasProvenance
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_provenance
;
np:hasPublicationInfo
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_assertion
a
np:Assertion
.
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_provenance
a
np:Provenance
.
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGNe3f8d58bba899f777ffcb5cee53b6561
sio:SIO_000628
miriam-gene:2099
,
lld:C0029456
;
a
sio:SIO_001122
.
}
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_provenance
{
dgn-np:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_assertion
dcterms:description
"[The specific XbaI and PvuII polymorphisms of the Er gene are associated with low bMD at all bMD measurement sites in the bulgarian female population.they might become useful genetic markers in osteoporosis risk assessment in this specific population.]. 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:17324916
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP124265.RAY79wBIotR7rogoqkd6CGqmi1sFYQCDROlfcJ2p55XyI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:04+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" .
}