@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY
> .
@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:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_head
{
this:
np:hasAssertion
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_assertion
;
np:hasProvenance
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_provenance
;
np:hasPublicationInfo
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_assertion
a
np:Assertion
.
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_provenance
a
np:Provenance
.
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGNbcc59509f038a937f38d819a0b8d62a2
sio:SIO_000628
miriam-gene:348
,
lld:C0023434
;
a
sio:SIO_001122
.
}
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_provenance
{
dgn-np:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_assertion
dcterms:description
"[The APOE allele and genotype distribution in these CLL patients is the same as in unaffected control populations, suggesting that although APOE genotype influences CLL outcome and response to therapy, it does not alter susceptibility to developing this disease.]. 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:18784741
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP71666.RAjHpnjroapM9bJX5xvQp_0unz1fp1iamkmFoi0AtPtkY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:34+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" .
}