@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo
> .
@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:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_head
{
this:
np:hasAssertion
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_assertion
;
np:hasProvenance
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_provenance
;
np:hasPublicationInfo
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_assertion
a
np:Assertion
.
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_provenance
a
np:Provenance
.
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0206701
a
ncit:C7057
.
dgn-gda:DGNb38c0307e4f3754ac5fd5c8127d00111
sio:SIO_000628
miriam-gene:672
,
lld:C0206701
;
a
sio:SIO_001121
.
}
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_provenance
{
dgn-np:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_assertion
dcterms:description
"[DNA ploidy and gene expression profile were used in order to compare gross genomic alteration and gene expression pattern between cases with BRCA1 loss through mutation, BRCA1 epigenetic loss, and no BRCA1 loss in cases of high-grade serous carcinoma with known BRCA1 and BRCA 2 status.]. 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:20843305
;
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:NP509872.RAPLzvLiUFwQdgN2ePzq42umk9OgRupPZqgQWZG0Y_Ebo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}