@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ
> .
@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:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_head
{
this:
np:hasAssertion
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_assertion
;
np:hasProvenance
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_assertion
a
np:Assertion
.
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_provenance
a
np:Provenance
.
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_assertion
{
miriam-gene:7040
a
ncit:C16612
.
lld:C0021364
a
ncit:C7057
.
dgn-gda:DGNd4e13f63de08166e3b7f4eeb9f740c2e
sio:SIO_000628
miriam-gene:7040
,
lld:C0021364
;
a
sio:SIO_001122
.
}
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_provenance
{
dgn-np:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_assertion
dcterms:description
"[Our results suggest that variant alleles of the five markers are absent or too rare to be useful genetic makers in Chinese, despite the fact that they have been commonly used as polymorphic markers in osteoporosis genetic research in other populations.]. 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:12491092
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP50629.RApNQb1SVBGPuCM46-g_lKKRJd88kftb1ulIh-UhixowQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}