@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI
> .
@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:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_head
{
this:
np:hasAssertion
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_assertion
;
np:hasProvenance
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_provenance
;
np:hasPublicationInfo
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_assertion
a
np:Assertion
.
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_provenance
a
np:Provenance
.
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_assertion
{
miriam-gene:10992
a
ncit:C16612
.
lld:C1516669
a
ncit:C7057
.
dgn-gda:DGN367e4b155a1dfc2ea184af3401728542
sio:SIO_000628
miriam-gene:10992
,
lld:C1516669
;
a
sio:SIO_001121
.
}
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_provenance
{
dgn-np:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_assertion
dcterms:description
"[In contrast, SF3B1 mutations have a lower incidence in early stages of chronic lymphocytic leukemia, are more common in advanced disease, and tend to be associated with poor prognosis, suggesting that they occur during clonal evolution of the disease.]. 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:23160465
;
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:NP308681.RAoVCuT2P2fqPaDsdpISdsms6JtilBpLvaMaxXy_c_3xI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}