@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_head
{
this:
np:hasAssertion
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_assertion
;
np:hasProvenance
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_assertion
a
np:Assertion
.
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_provenance
a
np:Provenance
.
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_assertion
{
miriam-gene:50964
a
ncit:C16612
.
lld:C0432273
a
ncit:C7057
.
dgn-gda:DGN78173c4d172fc996b0ec4dd8cdd56821
sio:SIO_000628
miriam-gene:50964
,
lld:C0432273
;
a
sio:SIO_001121
.
}
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_provenance
{
dgn-np:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_assertion
dcterms: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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP900154.RAEqIBVDu1jWjgD6rCW_mnqHvD36oOw4ydCO7POYo_e0o130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:49+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}