@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4
> .
@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:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_head
{
this:
np:hasAssertion
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion
;
np:hasProvenance
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance
;
np:hasPublicationInfo
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion
a
np:Assertion
.
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance
a
np:Provenance
.
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion
{
miriam-gene:79947
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN9438c44cb9a3acf98108e2639237aa8f
sio:SIO_000628
miriam-gene:79947
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance
{
dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion
dcterms:description
"[To determine the differences in DNA damage signalling leading to differential sensitivity to CPT, two human colon cancer cell lines, SW620 and KM12, with nonfunctional p53 and the same level of topoisomerase I cleavable complex formation but differential sensitivity to CPT (Cancer Res.]. 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:8938795
;
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:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:10+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" .
}