@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY
> .
@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:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_head
{
this:
np:hasAssertion
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_assertion
;
np:hasProvenance
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_provenance
;
np:hasPublicationInfo
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_assertion
a
np:Assertion
.
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_provenance
a
np:Provenance
.
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_assertion
{
miriam-gene:6573
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGN5becb25fed21dbe1d39149d9d9faa04c
sio:SIO_000628
miriam-gene:6573
,
lld:C0598608
;
a
sio:SIO_001121
.
}
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_provenance
{
dgn-np:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_assertion
dcterms:description
"[The purposes of this study were to explore whether hyperhomocysteinemia was related to MTX administration and toxicity and whether homocysteine or MTX toxicity differed by methylenetetrahydrofolate reductase (MTHFR) or reduced folate carrier (RFC) genetic polymorphisms.]. 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:12915598
;
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:NP215667.RA3IrlJMKyFS_xk76uhgHX9OoviGnrpcLbJQqNYxdEGNY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:59+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" .
}