@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY
> .
@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:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_head
{
this:
np:hasAssertion
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_assertion
;
np:hasProvenance
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_provenance
;
np:hasPublicationInfo
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_assertion
a
np:Assertion
.
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_provenance
a
np:Provenance
.
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_assertion
{
miriam-gene:56983
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNda8a8908292258c192173a6c0b2ca7d7
sio:SIO_000628
miriam-gene:56983
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_provenance
{
dgn-np:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_assertion
dcterms:description
"[Considering that hCLP46 has the capability of modifying the Notch pathway, our finding adds weight to the importance of Notch signaling in hematopoiesis and suggests that overexpression of hCLP46 might be an early event in the pathogenesis of AML and T-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:20143914
;
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:NP925763.RAdWlWk-o9k8gnyyUVYF-dEuS4vusFS62zo5EH0jZs8RY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:05+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" .
}