@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew
> .
@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:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_head
{
this:
np:hasAssertion
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_assertion
;
np:hasProvenance
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_provenance
;
np:hasPublicationInfo
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_assertion
a
np:Assertion
.
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_provenance
a
np:Provenance
.
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1378050
a
ncit:C7057
.
dgn-gda:DGN471ed70496d7e7ac848648d374ebd787
sio:SIO_000628
miriam-gene:595
,
lld:C1378050
;
a
sio:SIO_001121
.
}
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_provenance
{
dgn-np:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_assertion
dcterms:description
"[In this case, the correlation of the microscopic findings with changes in CCND1 gene associated to CCND1 overexpression in both components suggest that the ChRCC would have originated from the preexisting oncocytoma.]. 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:16337860
;
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:NP481020.RALjhDIcULmaRhqkLKWRfXc__YzCxVBU6xek4KBUaE9Ew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}