@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY
> .
@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 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:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_head
{
this:
np:hasAssertion
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_assertion
;
np:hasProvenance
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_provenance
;
np:hasPublicationInfo
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_assertion
a
np:Assertion
.
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_provenance
a
np:Provenance
.
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_assertion
{
miriam-gene:4041
a
ncit:C16612
.
lld:C1858556
a
ncit:C7057
.
dgn-gda:DGN6c1e4674a4363ec5331dc11e5260f885
sio:SIO_000628
miriam-gene:4041
,
lld:C1858556
;
a
sio:SIO_001121
.
}
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_provenance
{
dgn-np:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_assertion
dct:description
"[Other less common recessive or dominant sclerosing disorders, such as endosteal hyperostosis, sclerostosis, van Buchen disease and high bone mass syndrome, are due to mutations in two genes (LRP5 and SOST) of the Wnt pathway that induce increased osteoblast activity.]. 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:18328982
;
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:NP936520.RAFX5vsqsF7ewQ3UTgLSYooMi_SKCljD1TFOhrurgEAeY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:41:34+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}