@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk
> .
@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:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_head
{
this:
np:hasAssertion
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_assertion
;
np:hasProvenance
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_provenance
;
np:hasPublicationInfo
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_assertion
a
np:Assertion
.
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_provenance
a
np:Provenance
.
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C3160732
a
ncit:C7057
.
dgn-gda:DGNeb8381b9f0886737c617d6c6ed68a0f9
sio:SIO_000628
miriam-gene:3342
,
lld:C3160732
;
a
sio:SIO_001121
.
}
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_provenance
{
dgn-np:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) and conventional cytogenetic karyotyping were used to screen for losses and gains of DNA sequences along chromosomes in ten renal tumors (RCC) of different histologic types (clear-cell RCC, papillary RCC, and one 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:12377413
;
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:NP912806.RAGM7R5dq1ys57OEXk35pMCf1M93P-xVqeZIn-GJwogTk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}