@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM
> .
@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:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_head
{
this:
np:hasAssertion
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion
;
np:hasProvenance
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion
a
np:Assertion
.
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance
a
np:Provenance
.
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion
{
miriam-gene:4005
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN46709e1910365b8b121f880908d423cb
sio:SIO_000628
miriam-gene:4005
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_provenance
{
dgn-np:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_assertion
dcterms:description
"[The highly concordant nature of the genetic events giving rise to mouse and human leukemias with mutations at Lmo2 are an encouraging sign to those wanting to use mice to model human cancer and may help in designing safer methods for retroviral gene therapy.]. 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:19461887
;
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:NP574706.RAsRcO-cSXIoYawtDNke3O8i7aH6bMMnhbXqyneVOYrXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}