@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ
> .
@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/v4.0.0/void/
> .
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_head
{
this:
np:hasAssertion
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion
;
np:hasProvenance
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion
a
np:Assertion
.
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance
a
np:Provenance
.
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion
{
miriam-gene:26013
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGN2b3f0a0627081602b3d4691378cfd79a
sio:SIO_000628
miriam-gene:26013
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_provenance
{
dgn-np:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_assertion
dcterms:description
"[To examine whether L3MBTL functions as a classic TSG in human hematologic malignancies, we screened a panel of 17 myeloid leukemia cell lines and peripheral blood or bone marrow samples from 29 MDS and 13 MPD patients for mutations in the entire L3MBTL coding sequence, including intron/exon splice junctions.]. 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:15334543
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP457695.RAB1bmSh8BVpUJ9hNf2v69WfCj8FpkJ33tl8POohBXNEQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:12+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}