@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g
> .
@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:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_head
{
this:
np:hasAssertion
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion
;
np:hasProvenance
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance
;
np:hasPublicationInfo
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion
a
np:Assertion
.
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance
a
np:Provenance
.
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN4fe35f98d895f7b241d56c27295536e2
sio:SIO_000628
miriam-gene:1756
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_provenance
{
dgn-np:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_assertion
dcterms:description
"[Osteoporosis is a systemic disorder of decreased skeletal mass as measured by bone mineral density (BMD), and disturbed skeletal architecture and function which results in an increased risk for bone fractures with consecutively increased morbidity and mortality.]. 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:10812458
;
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:NP197282.RA8Pqt5Z2NC_7yvRberV_OQFit-xv15MilqbUkdl95D4g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}