@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw
> .
@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:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_head
{
this:
np:hasAssertion
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_assertion
;
np:hasProvenance
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_assertion
a
np:Assertion
.
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_provenance
a
np:Provenance
.
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_assertion
{
miriam-gene:1767
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGNc6aaf63d062b4f540b66cbcad5c3baf5
sio:SIO_000628
miriam-gene:1767
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_provenance
{
dgn-np:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_assertion
dcterms:description
"[Moreover, since defects in the pathway for PCD can render neoplastic cells resistant to the cytotoxic effects of chemotherapeutic drugs and radiation, investigations of the molecular biology of CLL may also prove informative for gaining a better understanding of drug- and radiation-resistance mechanisms.]. 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:9482522
;
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:NP257023.RAFdvAccPVf9Kr3IKwT02Fm0Jh47nmyBohVdOvqR0ggZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}