@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac
> .
@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:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_head
{
this:
np:hasAssertion
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion
;
np:hasProvenance
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance
;
np:hasPublicationInfo
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion
a
np:Assertion
.
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance
a
np:Provenance
.
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion
{
miriam-gene:50964
a
ncit:C16612
.
lld:C0432272
a
ncit:C7057
.
dgn-gda:DGNee49cb2553e0eb62872c99941b987047
sio:SIO_000628
miriam-gene:50964
,
lld:C0432272
;
a
sio:SIO_001121
.
}
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_provenance
{
dgn-np:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_assertion
dcterms:description
"[The exclusive bone phenotype of good quality of patients with sclerosteosis and Van Buchem disease and the specific localization of sclerostin make it an attractive target for the development of bone forming therapeutics.]. 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:15869900
;
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:NP467135.RAnlj3Tj-ULO_eISybm6VU8SAMHFc45rf97tuyoBrzVac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:40+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" .
}