@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_assertion
;
np:hasProvenance
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_provenance
;
np:hasPublicationInfo
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_assertion
a
np:Assertion
.
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_provenance
a
np:Provenance
.
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0334381
a
ncit:C7057
.
dgn-gda:DGN0c22f86a131d73b1060ebd81da17ab53
sio:SIO_000628
miriam-gene:3342
,
lld:C0334381
;
a
sio:SIO_001121
.
}
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_provenance
{
dgn-np:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_assertion
dcterms:description
"[In this study, we used microarray comparative genomic hybridization (CGH) to investigate genetic changes in atypical lobular hyperplasia (ALH) and lobular carcinoma in situ (LCIS), as the presence of these lobular neoplastic lesions is an indicator of risk in the development of invasive breast cancer.]. 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:16897748
;
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:NP666677.RADoY0k7r1WhtIrlo-Ve5OYduRLJFnGzeFIrDw-4eZzlw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
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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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}