@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU
> .
@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:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_head
{
this:
np:hasAssertion
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_assertion
;
np:hasProvenance
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_provenance
;
np:hasPublicationInfo
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_assertion
a
np:Assertion
.
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_provenance
a
np:Provenance
.
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNc610d12cb54b999cd4aa879ebddc6a19
sio:SIO_000628
miriam-gene:1728
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_provenance
{
dgn-np:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_assertion
dcterms:description
"[The NQO1 rs1800566 (C609T), PON1 rs854560 (L55M), and PON1 rs662 (Q192R) polymorphisms modified risk depending on leukemia subtype (decreased in AML, increased and decreased in ALL, respectively), age strata, and variant genotype combinations.]. 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:22976839
;
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:NP658693.RAdEC0VvJCANe-eTTt0FXMQEulKZ7Qabs3LmComunxUlU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:38+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" .
}