@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw
> .
@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:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_head
{
this:
np:hasAssertion
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_assertion
;
np:hasProvenance
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_assertion
a
np:Assertion
.
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_provenance
a
np:Provenance
.
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_assertion
{
miriam-gene:1043
a
ncit:C16612
.
lld:C0024419
a
ncit:C7057
.
dgn-gda:DGNcf63ee248fb4dffa30af1e80ed57fd41
sio:SIO_000628
miriam-gene:1043
,
lld:C0024419
;
a
sio:SIO_001123
.
}
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_provenance
{
dgn-np:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_assertion
dcterms:description
"[CD52 is widely expressed on human mast cells (MCs) and Waldenstrom's Macroglobulinemia bone marrow lymphoplasmacytic cells and provide the preclinical rationale for the use of alemtuzumab in the treatment of WM and possibly other MC-related disorders.]. 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:16796779
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP151476.RAJvQtIeGb34X6VFMZmO8NgDSN5dVxou8jkGBj-NGAnAw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:20+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" .
}