@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo
> .
@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:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_head
{
this:
np:hasAssertion
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_assertion
;
np:hasProvenance
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_provenance
;
np:hasPublicationInfo
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_assertion
a
np:Assertion
.
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_provenance
a
np:Provenance
.
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGN18b459f37ab550f5abb9b0c451a5a8bb
sio:SIO_000628
miriam-gene:2099
,
lld:C0024305
;
a
sio:SIO_001121
.
}
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_provenance
{
dgn-np:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_assertion
dcterms:description
"[(ii) A second region of 6q, which was distal to 6q23.1 (D6S238) and included ESR (6q25.1) and D6S281 (6q27), which was shown to be present in all our cases of ALL, was found to be deleted in 4 of the 7 cases of NHL.]. 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:7522544
;
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:NP660261.RAjd8ri_hgoSOFlIH-1azlgaQtocoT0vsftJF5LWaCLjo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}