@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A
> .
@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:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_head
{
this:
np:hasAssertion
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_assertion
;
np:hasProvenance
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_provenance
;
np:hasPublicationInfo
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_assertion
a
np:Assertion
.
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_provenance
a
np:Provenance
.
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_assertion
{
miriam-gene:4615
a
ncit:C16612
.
lld:C0026470
a
ncit:C7057
.
dgn-gda:DGNf459c6a4b01bd0945320b5d6eff57c61
sio:SIO_000628
miriam-gene:4615
,
lld:C0026470
;
a
sio:SIO_001122
.
}
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_provenance
{
dgn-np:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_assertion
dcterms:description
"[To our knowledge, this is the first case of del(5q) MDS following MGUS IgMk with the MYD88 L256P mutation in which there is coexistence of the markers of the two clonal diseases, but as an expression of distinct pathological features.]. 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:25159121
;
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:NP1214017.RAu7Mzl0Q-y5NJ4FDd3ELySsUcpBIw__rFifFpNEQNN_A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:56+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" .
}