@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk
> .
@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:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_head
{
this:
np:hasAssertion
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_assertion
;
np:hasProvenance
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_provenance
;
np:hasPublicationInfo
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_assertion
a
np:Assertion
.
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_provenance
a
np:Provenance
.
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_assertion
{
miriam-gene:10519
a
ncit:C16612
.
lld:C0023452
a
ncit:C7057
.
dgn-gda:DGN46d44c072fd362a289620b99dca97dd8
sio:SIO_000628
miriam-gene:10519
,
lld:C0023452
;
a
sio:SIO_001121
.
}
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_provenance
{
dgn-np:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_assertion
dcterms:description
"[In this report, we determined the exon organization of the TEL gene and performed mutational analysis of TEL and KIP1 in 33 childhood ALL patients known to have loss of heterozygosity at this locus.]. 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:8640833
;
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:NP676659.RAVh3Cami3GiaMV1KALuPC1ryiQWrCh8B8oVHCAIUPpuk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}