@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ
> .
@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:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_head
{
this:
np:hasAssertion
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_assertion
;
np:hasProvenance
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_assertion
a
np:Assertion
.
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_provenance
a
np:Provenance
.
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_assertion
{
miriam-gene:4041
a
ncit:C16612
.
lld:C0432272
a
ncit:C7057
.
dgn-gda:DGN243e9616b8ba243f3cf951598851417f
sio:SIO_000628
miriam-gene:4041
,
lld:C0432272
;
a
sio:SIO_001121
.
}
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_provenance
{
dgn-np:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_assertion
dcterms:description
"[The recent identification of a link between bone mass in humans and gain- or loss-of-function mutations in the Wnt coreceptor low-density lipoprotein receptor-related protein 5 (osteoporosis pseudoglioma syndrome, high bone mass trait) or in the Wnt antagonist sclerostin (sclerosteosis, van Buchem syndrome) has called the attention of academic and industry scientists and clinicians to the importance of this signaling pathway in skeletal biology and disease.]. 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:17395698
;
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:NP666443.RAeAWUwSMisTqLH2SlGVOJlqPkgui7JZvPh_x5wVeIqyQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}