@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI
> .
@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:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_head
{
this:
np:hasAssertion
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_assertion
;
np:hasProvenance
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_provenance
;
np:hasPublicationInfo
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_assertion
a
np:Assertion
.
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_provenance
a
np:Provenance
.
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_assertion
{
miriam-gene:6573
a
ncit:C16612
.
lld:C2697636
a
ncit:C7057
.
dgn-gda:DGN286780da531ba3c5743f88c1a2edc395
sio:SIO_000628
miriam-gene:6573
,
lld:C2697636
;
a
sio:SIO_001121
.
}
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_provenance
{
dgn-np:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_assertion
dcterms:description
"[This is on account of increased intracellular transport of MTX via the reduced folate carrier (RFC) whose gene is localized to chromosome 21 and may also account for the increased MTX-associated toxicity of DS ALL patients.]. 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:15390307
;
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:NP728453.RAO-57kmj9xaq90pQixlb22iHnXBF_rxfa99W75bssoOI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}