@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8
> .
@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:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_head
{
this:
np:hasAssertion
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_assertion
;
np:hasProvenance
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_provenance
;
np:hasPublicationInfo
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_assertion
a
np:Assertion
.
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_provenance
a
np:Provenance
.
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_assertion
{
miriam-gene:6965
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN5103467d2eb640545e27d8545670eab0
sio:SIO_000628
miriam-gene:6965
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_provenance
{
dgn-np:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_assertion
dcterms:description
"[These data indicate that the assignment of clonal specific markers based upon the sequence of TCRG rearrangements at presentation may not always be useful in the detection of minimal residual disease in ALL.]. 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:8289500
;
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:NP420490.RA3IWp97HsQZEUISfyS8ziRgVX6aq9pl57NZOQf1dyzD8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}