@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A
> .
@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:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_head
{
this:
np:hasAssertion
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_assertion
;
np:hasProvenance
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_assertion
a
np:Assertion
.
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_provenance
a
np:Provenance
.
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_assertion
{
miriam-gene:6955
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN84d51c21ca15a582dd823d51701c7eaf
sio:SIO_000628
miriam-gene:6955
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_provenance
{
dgn-np:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_assertion
dcterms:description
"[Southern blotting (SB) with multiple DNA probes for the IGH, IGK, TCRB, TCRG, TCRD and TAL1 loci revealed rearrangement patterns largely comparable to pediatric ALL, but several differences were found for precursor-B-ALL patients.]. 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:9665194
;
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:NP683959.RABpXF0LmcVz3GmMs4GIXb7bxwXvetcS1FwgMitbHYW8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}