@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao
> .
@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:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_head
{
this:
np:hasAssertion
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_assertion
;
np:hasProvenance
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_provenance
;
np:hasPublicationInfo
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_assertion
a
np:Assertion
.
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_provenance
a
np:Provenance
.
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_assertion
{
miriam-gene:632
a
ncit:C16612
.
lld:C0158447
a
ncit:C7057
.
dgn-gda:DGNd78aa97f53cfc516e109798659a5144b
sio:SIO_000628
miriam-gene:632
,
lld:C0158447
;
a
sio:SIO_001121
.
}
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_provenance
{
dgn-np:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_assertion
dcterms:description
"[The results are in agreement with previous histomorphologic studies indicating that men with idiopathic osteoporosis have an osteoblast dysfunction with decreased osteocalcin production and increased production of factors stimulating osteoclast activation.]. 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:16467976
;
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:NP794147.RAYDj_jY-HIwfYAf54YeQbeeda4dnXizkgLv3PQGwwlao130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:07+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" .
}