@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY
> .
@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:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_head
{
this:
np:hasAssertion
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_assertion
;
np:hasProvenance
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_provenance
;
np:hasPublicationInfo
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_assertion
a
np:Assertion
.
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_provenance
a
np:Provenance
.
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNc6f1ff7b9009935f7d25601074f61632
sio:SIO_000628
miriam-gene:4524
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_provenance
{
dgn-np:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_assertion
dcterms:description
"[A case control study was conducted on Brazilian children in different regions of the country with the aim of investigating the role of MTHFR C677T and A1298C polymorphisms as risk factors in the development of acute myeloid leukemia (AML).]. 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:17071478
;
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:NP784514.RACLbowc1HHC765UJE71oOLBc5pCfJU_S9PXYCcBY57VY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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
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"v2.1.0" .
}