@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8
> .
@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:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_head
{
this:
np:hasAssertion
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_assertion
;
np:hasProvenance
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_provenance
;
np:hasPublicationInfo
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_assertion
a
np:Assertion
.
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_provenance
a
np:Provenance
.
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_assertion
{
miriam-gene:28639
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN0043848a390739529f55c5bdb8e317ee
sio:SIO_000628
miriam-gene:28639
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_provenance
{
dgn-np:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_assertion
dcterms:description
"[We found that TCRB and TCRG HTS not only identified clonality at diagnosis in most cases (31 of 43 for TCRB and 27 of 43 for TCRG) but also detected subsequent MRD.]. 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:22593176
;
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:NP314943.RA5WVQ06ZKIHdWH8pe8vrx9lfu_nL_NKoWNpEgZuxx7h8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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" .
}