@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA
> .
@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:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_head
{
this:
np:hasAssertion
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_assertion
;
np:hasProvenance
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_provenance
;
np:hasPublicationInfo
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_assertion
a
np:Assertion
.
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_provenance
a
np:Provenance
.
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_assertion
{
miriam-gene:51135
a
ncit:C16612
.
lld:C1333296
a
ncit:C7057
.
dgn-gda:DGNc69fcd0d282bc18d278ff1ba8f35f75e
sio:SIO_000628
miriam-gene:51135
,
lld:C1333296
;
a
sio:SIO_001121
.
}
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_provenance
{
dgn-np:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_assertion
dcterms:description
"[Hence, the MYD88 signalling pathway is integral to the pathogenesis of ABC DLBCL, supporting the development of inhibitors of IRAK4 kinase and other components of this pathway for the treatment of tumours bearing oncogenic MYD88 mutations.]. 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:21179087
;
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:NP537150.RA9q1HARMawKPuDc_oAi3Hhq1qJa_MocPC7Hu6r2AhNdA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}