@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA
> .
@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:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_head
{
this:
np:hasAssertion
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_assertion
;
np:hasProvenance
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_provenance
;
np:hasPublicationInfo
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_assertion
a
np:Assertion
.
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_provenance
a
np:Provenance
.
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_assertion
{
miriam-gene:50964
a
ncit:C16612
.
lld:C0432272
a
ncit:C7057
.
dgn-gda:DGN4ee449334074075aef1f8d29a7a3dc6e
sio:SIO_000628
miriam-gene:50964
,
lld:C0432272
;
a
sio:SIO_001121
.
}
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_provenance
{
dgn-np:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_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-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:NP589982.RAL5UK0xI6_cJps04mNwPAAnpypjIP1dzRkx_AWgKVhzA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}