@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ
> .
@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:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_head
{
this:
np:hasAssertion
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_assertion
;
np:hasProvenance
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_assertion
a
np:Assertion
.
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_provenance
a
np:Provenance
.
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_assertion
{
miriam-gene:6343
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGN8adbe9a29cda8c5293b56237e1c760ab
sio:SIO_000628
miriam-gene:6343
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_provenance
{
dgn-np:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_assertion
dcterms:description
"[In order to ascertain whether the organ-system tropism of AL was associated with immunoglublin light chain variable region (Ig VL) germline gene utilization, we attempted to clone, sequence and assign germline donors to the clonal Ig VL genes of 62 AL patients, all of whom were treated with SCT.]. 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:10468868
;
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:NP553148.RAZq5MN5HcE37M4A8ahGnpfbSSD2bP11aCIiCPEGc4EhQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}