@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E
> .
@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/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_assertion
a
np:Assertion
.
dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_provenance
a
np:Provenance
.
dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_publicationInfo
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.
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{
miriam-gene:4615
a
ncit:C16612
.
lld:C0024419
a
ncit:C7057
.
dgn-gda:DGNe2e2766f41cc48ba76005b09a806fa08
sio:SIO_000628
miriam-gene:4615
,
lld:C0024419
;
a
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.
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dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_provenance
{
dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_assertion
dcterms:description
"[We performed a prospective study of ibrutinib in 63 symptomatic patients with Waldenström's macroglobulinemia who had received at least one previous treatment, and we investigated the effect of MYD88 and CXCR4 mutations on outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:25853747
;
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 .
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dgn-np:NP1276559.RA_uVNtxYYPai_7XiCxPd6BUUCafeK1bCeGjRZHYIg69E130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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> , <
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" .
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"v4.0.0" .
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