@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ
> .
@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:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_head
{
this:
np:hasAssertion
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_assertion
;
np:hasProvenance
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_assertion
a
np:Assertion
.
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_provenance
a
np:Provenance
.
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGNf4462a3a7f1d306917fd9197ed890736
sio:SIO_000628
miriam-gene:595
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_provenance
{
dgn-np:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_assertion
dcterms:description
"[To understand the dynamics of genomic alterations in this progression, we used four multicolor fluorescence in situ hybridization probe panels consisting of the oncogenes COX2, MYC, HER2, CCND1, and ZNF217 and the tumor suppressor genes DBC2, CDH1, and TP53 to visualize copy number changes in 13 cases of synchronous DCIS and IDC based on single-cell analyses.]. 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:23062488
;
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:NP194116.RAVofiuvwy5v3qZDH0X7jbpvhC9IEmLheyMFST3Pm-oJQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}