@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo
> .
@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:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_head
{
this:
np:hasAssertion
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_assertion
;
np:hasProvenance
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_provenance
;
np:hasPublicationInfo
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_assertion
a
np:Assertion
.
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_provenance
a
np:Provenance
.
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGNd1f1485b9c49b704c4b0272b085c33bb
sio:SIO_000628
miriam-gene:4524
,
lld:C1961102
;
a
sio:SIO_001122
.
}
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_provenance
{
dgn-np:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_assertion
dcterms:description
"[We conducted a case-control study in 95 north Indian children with acute lymphoblastic leukemia (ALL) and 255 controls, to investigate the role of MTHFR C677T and A1298C polymorphisms as risk factors in the development of ALL.]. 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:20367562
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP69372.RA_rdYLq_VrSoDPXFKw7dbNIuYA6WWqrMG6mx4ZmhsOoo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:33+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" .
}