@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o
> .
@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:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_head
{
this:
np:hasAssertion
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion
;
np:hasProvenance
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion
a
np:Assertion
.
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance
a
np:Provenance
.
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0242621
a
ncit:C7057
.
dgn-gda:DGN2bd6f5767279ac4d8c7d6420c514aab9
sio:SIO_000628
miriam-gene:3342
,
lld:C0242621
;
a
sio:SIO_001121
.
}
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_provenance
{
dgn-np:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) revealed regions of gains and amplification in three locations, with gains of chromosome 7, amplification of 8q24 (corresponding to the MYCC locus) and gains of the long arm of chromosome 17 (suggestive of isochromosome 17q).]. 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:10643003
;
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:NP797727.RAvfRrrCvAilSDtPbSg7LdrcALI_khWfNES23aVD0As5o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}