@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how
> .
@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:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_head
{
this:
np:hasAssertion
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_assertion
;
np:hasProvenance
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_provenance
;
np:hasPublicationInfo
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_assertion
a
np:Assertion
.
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_provenance
a
np:Provenance
.
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_assertion
{
miriam-gene:4015
a
ncit:C16612
.
lld:C0035086
a
ncit:C7057
.
dgn-gda:DGN3c4a6f4ea02483e9a5998269a3110642
sio:SIO_000628
miriam-gene:4015
,
lld:C0035086
;
a
sio:SIO_001121
.
}
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_provenance
{
dgn-np:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_assertion
dcterms:description
"[These observations provide clues to ROD pathogenesis, as they indicate that the suppression of osteoblast differentiation and decreased active LOX protein associated with accumulation of AGEs in osteoblasts caused structural abnormalities of bone collagen fibrils and a severe mineralization disorder, leading to bone fragility.]. 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:23979426
;
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:NP197249.RAjspaHGLVyAgh-sHL3TBy9yDew2Z-iP-7MIoP64u9how130_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" .
}