@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8
> .
@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:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_head
{
this:
np:hasAssertion
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_assertion
;
np:hasProvenance
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_provenance
;
np:hasPublicationInfo
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_assertion
a
np:Assertion
.
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_provenance
a
np:Provenance
.
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_assertion
{
miriam-gene:290
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN1d2a130c1cc6a1f275d593e8235109e8
sio:SIO_000628
miriam-gene:290
,
lld:C0023434
;
a
sio:SIO_001123
.
}
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_provenance
{
dgn-np:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_assertion
dcterms:description
"[Data suggest that detection of CD2 or CD13 expression in chronic lymphocytic leukemia (CLL) suggests familial CLL, and that CD38 expression does not carry the negative prognosis observed in sporadic CLL.]. 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:18431797
;
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:NP133715.RAdgTnxVHNxM-xnmyKEETkc_PM-erxgzm-yMiPXBu_SN8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:09+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" .
}