@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc
> .
@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:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_head
{
this:
np:hasAssertion
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion
;
np:hasProvenance
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance
;
np:hasPublicationInfo
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion
a
np:Assertion
.
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance
a
np:Provenance
.
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0007124
a
ncit:C7057
.
dgn-gda:DGNcf4c3eb598cfdaf3792d8091d81bc358
sio:SIO_000628
miriam-gene:3342
,
lld:C0007124
;
a
sio:SIO_001121
.
}
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_provenance
{
dgn-np:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_assertion
dcterms:description
"[Comparative genomic hybridization (CGH) was used to compare chromosomal alterations in 18 initial DCIS lesions (presenting in the absence of invasive disease) and in their subsequent ipsilateral DCIS recurrences (detected from 16 months to 9.3 years later).]. 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:10675380
;
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:NP208911.RAkq_F2n7ujnDOcdzwCSD-eo6JXUDRLOF60tUr4u84xLc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}