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http://rdf.disgenet.org/nanopublications.trig#NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao
> .
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> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_assertion
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np:hasProvenance
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dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_assertion
a
np:Assertion
.
dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_provenance
a
np:Provenance
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dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_publicationInfo
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{
miriam-gene:4524
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN1b51f6887224835de306a8820c569a15
sio:SIO_000628
miriam-gene:4524
,
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.
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dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_provenance
{
dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_assertion
dcterms:description
"[We analysed common genetic polymorphisms of 5,10-methylenetetrahydrofolate reductase (MTHFR), thymidylate synthase (TS), methionine synthase (MS) and methionine synthase reductase (MTRR) in 68 children with ALL and 258 healthy controls to investigate their influence on the risk for ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:17454638
;
prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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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 .
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dgn-np:NP185119.RAAYEHXWFtlrOBi4u7n1Nvu7MAlxSN9PjIogl3FsFDXao130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> , <
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pav:createdBy
<
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