@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_head
{
this:
np:hasAssertion
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion
;
np:hasProvenance
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance
;
np:hasPublicationInfo
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion
a
np:Assertion
.
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance
a
np:Provenance
.
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN661959b82a4383a405d6b122d0fe63fb
sio:SIO_000628
miriam-gene:4524
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_provenance
{
dgn-np:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_assertion
dcterms:description
"[No significant associations between specific MTHFR variants or combinations of variants and risk of ALL were observed neither in the total patient group nor in analyses stratified by gender, age at diagnosis, DNA index, immunophenotype, or TEL/AML1 rearrangement.]. 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:15921520
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP496842.RAKLGSQAD7cMyYAO1ro5Xhls7c_L3f3Uy9L5DVEQGM5So130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:30+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}