@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I
> .
@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:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_head
{
this:
np:hasAssertion
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_assertion
;
np:hasProvenance
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_provenance
;
np:hasPublicationInfo
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_assertion
a
np:Assertion
.
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_provenance
a
np:Provenance
.
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN002323ba226833d182bd826e20178dd8
sio:SIO_000628
miriam-gene:3342
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_provenance
{
dgn-np:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_assertion
dcterms:description
"[In order to gain more detailed insights into cytogenetic mechanisms of the pathogenesis of breast cancer, the chromosomal imbalances of 206 invasive breast cancer cases were characterised by means of comparative genomic hybridisation (CGH).]. 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:15054466
;
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:NP249328.RAiTCk5pE0n86dzqWargHexX4xDs2JcFx3dlso0Fic24I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}