@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs
> .
@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/v4.0.0/void/
> .
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_head
{
this:
np:hasAssertion
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion
;
np:hasProvenance
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance
;
np:hasPublicationInfo
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion
a
np:Assertion
.
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance
a
np:Provenance
.
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0029456
a
ncit:C7057
.
dgn-gda:DGN970f7232317ba0b08e40e7146a59c7f9
sio:SIO_000628
miriam-gene:1756
,
lld:C0029456
;
a
sio:SIO_001121
.
}
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_provenance
{
dgn-np:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_assertion
dcterms:description
"[Mutations in the LRP5 gene on chromosome 11q12-13 have been associated with rare syndromes characterized by extremely low or high BMD, but little is known about the contribution of this gene to the development of osteoporosis and determination of BMD in a normal population.]. 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:15355556
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP459032.RAUaf56vjxqWZH9tpJ_6y_9HpFwxGpfs3HD73WEsxwGYs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:13+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}