@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_assertion
a
np:Assertion
.
dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_provenance
a
np:Provenance
.
dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7124
a
ncit:C16612
.
lld:C0002382
a
ncit:C7057
.
dgn-gda:DGN1efa9424e992dc89aeedbb926da0cb48
sio:SIO_000628
miriam-gene:7124
,
lld:C0002382
;
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.
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dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_provenance
{
dgn-np:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_assertion
dcterms:description
"[These results suggest a molecular phenotype in which discrete sets of differentially expressed genes are associated with genetically determined susceptibility (Il1b, Tnf, and Stat6) or resistance (Il15 and Selp) to alveolar bone loss, providing insight into the genetic etiology of this complex 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:15271905
;
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:NP592229.RArZL7QpwJyU2oJhfGQuMxqCqc2MYHha-di1mH8k3qBtU130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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