@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck
> .
@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:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_head
{
this:
np:hasAssertion
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_assertion
;
np:hasProvenance
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_provenance
;
np:hasPublicationInfo
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_assertion
a
np:Assertion
.
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_provenance
a
np:Provenance
.
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_assertion
{
miriam-gene:958
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN22481d8f4dad5b8bbbde4cfce4ee551a
sio:SIO_000628
miriam-gene:958
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_provenance
{
dgn-np:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_assertion
dcterms:description
"[Women with the TT genotype in rs1883832 SNP affecting to Kozak consensus sequence of CD40 gene had lower BMD at FN and at LS sites and increased risk of osteopenia or osteoporosis.]. 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:18097708
;
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:NP790262.RA3NfeMto6dwg54GBrOsvUIHVFqMXUtI9fHvXLg_lx6ck130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}