@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI
> .
@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:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_head
{
this:
np:hasAssertion
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_assertion
;
np:hasProvenance
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_provenance
;
np:hasPublicationInfo
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_assertion
a
np:Assertion
.
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_provenance
a
np:Provenance
.
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_assertion
{
miriam-gene:4580
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN4d6ca4ad58acc8c5158a4f553d9341cd
sio:SIO_000628
miriam-gene:4580
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_provenance
{
dgn-np:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_assertion
dcterms:description
"[The relevance of this phenomenon in clinical samples is unknown but is extremely pertinent in childhood acute lymphoblastic leukaemia (ALL) in which children are exposed for prolonged periods to both MTX and thiopurines such that a single amplification event involving both the DHFR and the MSH3 genes may cause chemotherapeutic resistance to both agents.]. 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:17148505
;
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:NP430719.RAmf6Mlh08RbOjHILhkv_OinpnI4eedmwNoBG_yYz_FdI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}