@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc
> .
@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:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_head
{
this:
np:hasAssertion
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_assertion
;
np:hasProvenance
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_provenance
;
np:hasPublicationInfo
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_assertion
a
np:Assertion
.
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_provenance
a
np:Provenance
.
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_assertion
{
miriam-gene:6239
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN8fb37a7c79f661dfcb7e617b10022680
sio:SIO_000628
miriam-gene:6239
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_provenance
{
dgn-np:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_assertion
dcterms:description
"[Using a four-probe fluorescence in situ hybridization (FISH) assay targeting RREB1, MYB, Cep6, and CCND1, we found that seven of the eight propositus cases showed chromosomal aberrations consistent with the standardized FISH diagnostic criteria for melanoma.]. 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:22892832
;
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:NP769732.RA36PAOyQhvdA_aLXrJVLvT-9Ik6VAOwF3JP1uKQSNZcc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}