@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4
> .
@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:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_head
{
this:
np:hasAssertion
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion
;
np:hasProvenance
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance
;
np:hasPublicationInfo
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion
a
np:Assertion
.
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance
a
np:Provenance
.
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion
{
miriam-gene:3492
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNc925caecc821842e3c2e4d009adb3d9e
sio:SIO_000628
miriam-gene:3492
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_provenance
{
dgn-np:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_assertion
dcterms:description
"[To assess the frequency of the t(4;14)(p16.3;q32) translocation in MM, we performed a double-color fluorescent in situ hybridization (FISH) analysis of interphase nuclei with differently labeled probes specific for the IGH locus (a pool of plasmid clones specific for the IGH constant regions) or 4p16.3 (yeast artificial chromosome (YAC) 764-H1 spanning the region involved in breakpoints).]. 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:10397739
;
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:NP326758.RA9iDjOMX7SZl05CRhlHIOopxgD4tSdqMRbsICpcUPgD4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:11+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" .
}