@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs
> .
@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:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_head
{
this:
np:hasAssertion
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_assertion
;
np:hasProvenance
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_provenance
;
np:hasPublicationInfo
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_assertion
a
np:Assertion
.
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_provenance
a
np:Provenance
.
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_assertion
{
miriam-gene:50964
a
ncit:C16612
.
lld:C2678504
a
ncit:C7057
.
dgn-gda:DGN61573d9c954f672465c01dbc49e7a713
sio:SIO_000628
miriam-gene:50964
,
lld:C2678504
;
a
sio:SIO_001121
.
}
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_provenance
{
dgn-np:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_assertion
dcterms:description
"[Among the most distinctly expressed genes were Wnt antagonists DKK1 and SOST, the transcription factor SOX4, and the bone matrix proteins MMP13 and MEPE, all reduced in osteoporosis versus control groups.]. 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:21452281
;
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:NP743657.RAbG254IlpjnL9IObdkJgRr9gL3UCzeSquh_BEQLR6ifs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}