@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_head
{
this:
np:hasAssertion
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_assertion
;
np:hasProvenance
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_provenance
;
np:hasPublicationInfo
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_assertion
a
np:Assertion
.
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_provenance
a
np:Provenance
.
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_assertion
{
miriam-gene:4005
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGN0a5d9570bc1f044c63edca83af50dc07
sio:SIO_000628
miriam-gene:4005
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_provenance
{
dgn-np:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP538122.RAkkXb-pT9UkBHl3xsfy8bvptDR1lyA1e9FdzkJKP7PYE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:58+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}