@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM
> .
@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:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_head
{
this:
np:hasAssertion
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion
;
np:hasProvenance
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance
;
np:hasPublicationInfo
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion
a
np:Assertion
.
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance
a
np:Provenance
.
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion
{
miriam-gene:7301
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNfb4dab4d63c4f69d8c06a90653bfd7fc
sio:SIO_000628
miriam-gene:7301
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_provenance
{
dgn-np:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_assertion
dcterms:description
"[To characterize the genomic instability observed in these tumors, to establish a comparative map of chromosomal imbalances and to contribute to the validation of this mouse model of breast cancer, we have characterized chromosomal imbalances and aberrations using comparative genomic hybridization (CGH), and spectral karyotyping (SKY).]. 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:12140760
;
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:NP915836.RA0FBV8egKwRu0_wtijDNB5VUuHUg_7FLmw6GuTNDltMM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}