@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow
> .
@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:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_head
{
this:
np:hasAssertion
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_assertion
;
np:hasProvenance
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_provenance
;
np:hasPublicationInfo
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_assertion
a
np:Assertion
.
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_provenance
a
np:Provenance
.
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_assertion
{
miriam-gene:2317
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN568aa8f6ed47ce435502748421f1ee99
sio:SIO_000628
miriam-gene:2317
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_provenance
{
dgn-np:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_assertion
dcterms:description
"[These translocations and unique immunoglobulin rearrangements provide clonal markers of disease that can be amplified with the polymerase chain reaction (PCR), allowing detection and assessment of the clinical significance of minimal residual disease (MRD) after 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:9672773
;
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:NP309343.RA8zPagQsWGWpD9J-_11EMwNd-jmdi93i8X_Urf6nQIow130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}