@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU
> .
@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:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_head
{
this:
np:hasAssertion
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_assertion
;
np:hasProvenance
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_assertion
a
np:Assertion
.
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_provenance
a
np:Provenance
.
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN51da5f546e6729aaa5f42b3720cdec47
sio:SIO_000628
miriam-gene:5925
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_provenance
{
dgn-np:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_assertion
dcterms:description
"[The subchromosomal region frequently altered in lymphoma on 13q14 is the region around RB1 locus and centromeric to D13S319 locus, which is an overlapped region frequently deleted in chronic lymphocytic leukemia.]. 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:10374885
;
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:NP436428.RA2VUnv1P5dnFbgOuuU5sI3jLYv2FUdzndrZgH7537aYU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}