@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA
> .
@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:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_head
{
this:
np:hasAssertion
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_assertion
;
np:hasProvenance
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_provenance
;
np:hasPublicationInfo
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_assertion
a
np:Assertion
.
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_provenance
a
np:Provenance
.
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_assertion
{
miriam-gene:7439
a
ncit:C16612
.
lld:C0221002
a
ncit:C7057
.
dgn-gda:DGNd24b787a7f30f8530eaa0f7f6f807d90
sio:SIO_000628
miriam-gene:7439
,
lld:C0221002
;
a
sio:SIO_001121
.
}
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_provenance
{
dgn-np:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_assertion
dcterms:description
"[On the other hand, there was no association between Dra II polymorphism and BMD in both controls and pHPT patients, but serum intact PTH level was significantly higher in DD genotype than Dd/dd genotype in pHPT patients.]. 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:10468923
;
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:NP238460.RA_aYjOescBBXI7BWiVt358iV1kDMNkLcUWIQjFxqKGoA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}