@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk
> .
@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:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_head
{
this:
np:hasAssertion
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_assertion
;
np:hasProvenance
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_provenance
;
np:hasPublicationInfo
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_assertion
a
np:Assertion
.
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_provenance
a
np:Provenance
.
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1332629
a
ncit:C7057
.
dgn-gda:DGNff424572a75ef841f01eb28ccc67dea2
sio:SIO_000628
miriam-gene:3342
,
lld:C1332629
;
a
sio:SIO_001121
.
}
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_provenance
{
dgn-np:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_assertion
dcterms:description
"[In this study, comparative genomic hybridization (CGH) was used to screen ductal hyperplasia and other BPBD lesions and ductal carcinoma in situ (DCIS) for common genomic abnormalities, to test the relationship between these hyperplastic and neoplastic lesions.]. 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:11745672
;
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:NP932648.RAOGG5xeOFkL7VKLutOEYTayO3NQ5wIm0Lzrhs7mxGuIk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}