@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA
> .
@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:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_head
{
this:
np:hasAssertion
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_assertion
;
np:hasProvenance
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_provenance
;
np:hasPublicationInfo
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_assertion
a
np:Assertion
.
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_provenance
a
np:Provenance
.
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_assertion
{
miriam-gene:6461
a
ncit:C16612
.
lld:C1868682
a
ncit:C7057
.
dgn-gda:DGN2b160af148417212df354cf96a9fc447
sio:SIO_000628
miriam-gene:6461
,
lld:C1868682
;
a
sio:SIO_001121
.
}
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_provenance
{
dgn-np:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_assertion
dcterms:description
"[The comparative analysis of gene expression in either set of cell lines allowed the identification of four genes (RCCl, IFI16, hox2 and h19) preferentially transcribed in sensitive cells and two (SHB and PKC-zeta) preferentially expressed in resistant cells.]. 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:12079243
;
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:NP403750.RAPT0GtoqMzU3CrmdtsI83U37wFcCUVrKVfkcuhR7IoHA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}