@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM
> .
@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:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_head
{
this:
np:hasAssertion
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_assertion
;
np:hasProvenance
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_provenance
;
np:hasPublicationInfo
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_assertion
a
np:Assertion
.
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_provenance
a
np:Provenance
.
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_assertion
{
miriam-gene:28461
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN23c967d1bcb5ea5f81625d0375d41a72
sio:SIO_000628
miriam-gene:28461
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_provenance
{
dgn-np:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_assertion
dcterms:description
"[We analyzed the immunoglobulin (Ig) variable heavy (IGHV) and variable light chain genes used by leukemia cells of 258 unrelated patients with chronic lymphocytic leukemia (CLL) found to express unmutated Ig heavy chains (IgH) encoded by a 51p1 allele of IGHV1-69 among 1846 CLL patients examined.]. 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:17675554
;
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:NP752912.RAoaJGlMvxU0nLHJU7mrDb5f8Ug3NCV2DoBOFWwEyREsM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}