@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI
> .
@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:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_head
{
this:
np:hasAssertion
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_assertion
;
np:hasProvenance
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_provenance
;
np:hasPublicationInfo
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_assertion
a
np:Assertion
.
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_provenance
a
np:Provenance
.
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_assertion
{
miriam-gene:1378
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN5ea37f7bb574f608618e53a7ee42be49
sio:SIO_000628
miriam-gene:1378
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_provenance
{
dgn-np:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_assertion
dcterms:description
"[In the review, the risks and benefits of these choices are discussed to determine whether and by what means to proceed to HSCT in adult patients with ALL who are in CR1.]. 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:18024663
;
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:NP222993.RAf7mdbmkKW9eI1J-Ivjw1g6bINmJ5gq_lRkc3hyfmqxI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}