@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY
> .
@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:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_head
{
this:
np:hasAssertion
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_assertion
;
np:hasProvenance
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_provenance
;
np:hasPublicationInfo
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_assertion
a
np:Assertion
.
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_provenance
a
np:Provenance
.
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN7599638a728ed6feefd8e81d2d784d7b
sio:SIO_000628
miriam-gene:57026
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_provenance
{
dgn-np:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_assertion
dcterms:description
"[In an attempt to elucidate these etiological and phenotypic complexities, the present study, based on the fundamental concept that genomic instability is the engine of both tumor progression and tumor heterogeneity, was conducted to test the hypothesis that breast cancer pathogenesis is driven by double-strand break (DSB)-initiated chromosome instability (CIN).]. 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:10919664
;
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:NP670183.RA7LhQ1K3rlLEsT5XV1MLSU5vSiJHqYiDaU1OsaNFTUyY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}