@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA
> .
@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:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_head
{
this:
np:hasAssertion
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_assertion
;
np:hasProvenance
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_provenance
;
np:hasPublicationInfo
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_assertion
a
np:Assertion
.
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_provenance
a
np:Provenance
.
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_assertion
{
miriam-gene:3586
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGN394c4c836f7be542ec639f15aa845e51
sio:SIO_000628
miriam-gene:3586
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_provenance
{
dgn-np:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_assertion
dcterms:description
"[The FLT3 molecular marker is listed as a prognostic factor, an important leukaemogenic marker in acute leukemias, also the polymorphism (G1082A) of the IL10 interleukin can to present pleiotropic effects in many diseases and could is associated to 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:23086275
;
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:NP228448.RA6O6PS6BZqNYJdSRroHSsZ7ne3kNLxNjH7dkWxavM6MA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}