@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus
> .
@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:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_head
{
this:
np:hasAssertion
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_assertion
;
np:hasProvenance
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_provenance
;
np:hasPublicationInfo
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_assertion
a
np:Assertion
.
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_provenance
a
np:Provenance
.
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_assertion
{
miriam-gene:50715
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN0d3fbecaf857f1ba9a75f86ae89a50aa
sio:SIO_000628
miriam-gene:50715
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_provenance
{
dgn-np:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_assertion
dcterms:description
"[Notably, structure-function analysis of leukemia-derived and synthetic JME mutants demonstrated that the aberrant activation of NOTCH1 signaling is dependent on the number of residues introduced in the extracellular juxtamembrane region of the receptor and not on the specific amino acid sequence of these insertions.]. 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:18411416
;
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:NP326187.RA454CvwKFxTKokczg-3TFy93MJw9ByZ5SbDQrMq7_vus130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}