@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs
> .
@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:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_head
{
this:
np:hasAssertion
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion
;
np:hasProvenance
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion
a
np:Assertion
.
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance
a
np:Provenance
.
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion
{
miriam-gene:25
a
ncit:C16612
.
lld:C0751606
a
ncit:C7057
.
dgn-gda:DGN558529c9292167e727d4bfebf3e99328
sio:SIO_000628
miriam-gene:25
,
lld:C0751606
;
a
sio:SIO_001121
.
}
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_provenance
{
dgn-np:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_assertion
dcterms:description
"[The diagnosis of the BCR-ABL fusion gene in ALL has important clinical implications because it is the most common molecular genetic change in adult ALL and is associated with short remissions and poor outcome in all age groups.]. 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:1516023
;
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:NP445330.RABbM1jpoeYq5MtwKxRwtHqHa4GW9obgqRgyNNZG_ASKs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:07+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" .
}