@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI
> .
@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:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_head
{
this:
np:hasAssertion
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion
;
np:hasProvenance
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance
;
np:hasPublicationInfo
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion
a
np:Assertion
.
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance
a
np:Provenance
.
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion
{
miriam-gene:112399
a
ncit:C16612
.
lld:C0024419
a
ncit:C7057
.
dgn-gda:DGN71d043800a7b65c9a676292be05e6019
sio:SIO_000628
miriam-gene:112399
,
lld:C0024419
;
a
sio:SIO_001121
.
}
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_provenance
{
dgn-np:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_assertion
dcterms:description
"[Analyses of a well-characterised series of cases of plasma cell dyscrasias, including multiple myeloma (MM), Waldenström's macroglobulinaemia (WM) and monoclonal gammopathy of undetermined significance (MGUS) surprisingly demonstrated that the CpG island of EGLN3, and not EGLN1, is frequently methylated in these disorders.]. 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:19737309
;
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:NP549790.RAD73s54849bFQNatOCtTyUf0NClxb6X-3UFJ3h-TG4GI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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
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"v2.1.0" .
}