@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g
> .
@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:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_head
{
this:
np:hasAssertion
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion
;
np:hasProvenance
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance
;
np:hasPublicationInfo
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion
a
np:Assertion
.
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance
a
np:Provenance
.
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN0cef32bda86f15449a97bf3596f4dde1
sio:SIO_000628
miriam-gene:4023
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_provenance
{
dgn-np:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_assertion
dcterms:description
"[Higher LPL level was found in patients with unfavorable cytogenetic aberrations (deletion in 17p13 or 11q22) in contrast to lower level in good risk cytogenetics (deletion in 13q as the sole abnormality) (r = 0.404, P = 0.002).]. 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:18616755
;
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:NP372295.RAPuDwK8nM4iSv_fek7zBJycpCayAfcBj9JgAcbZ7IJ-g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+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" .
}