@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE
> .
@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:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_head
{
this:
np:hasAssertion
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_assertion
;
np:hasProvenance
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_provenance
;
np:hasPublicationInfo
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_assertion
a
np:Assertion
.
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_provenance
a
np:Provenance
.
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_assertion
{
miriam-gene:924
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN23d918ec2559b0a8c4ef2ec3d7db5bd4
sio:SIO_000628
miriam-gene:924
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_provenance
{
dgn-np:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_assertion
dcterms:description
"[The role of the MDR phenotype in clinical resistance is also not clearly demonstrated, because of the frequent association of other markers of bad prognosis on the same subset of cells (CD34, CD7 in leukemia).]. 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:7642463
;
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:NP475952.RAr3uQcUmcU8LHiNH_99psoiP8ta-KBQGOWo2iZXnJEUE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}