@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ
> .
@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:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_head
{
this:
np:hasAssertion
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion
;
np:hasProvenance
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion
a
np:Assertion
.
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance
a
np:Provenance
.
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN6357bb923447a7d739d4c33699e6ddae
sio:SIO_000628
miriam-gene:920
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_provenance
{
dgn-np:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_assertion
dcterms:description
"[Upon comparing the clinical and haematological disease characteristics of hyperdiploid versus diploid cases, the former group was characterized by a lower age, reduced incidence of anaemia, lower beta 2M levels, higher proliferative activity within the residual normal haemopoietic cells, increased expression of CD56 antigen in PC, and higher proportion of PB CD4+ T cells.]. 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:7786771
;
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:NP404327.RAn91VsCel7mxpMjn2qUiZzQ7GJRmmPz2FoxdJwq_LThQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}