@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA
> .
@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:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_head
{
this:
np:hasAssertion
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_assertion
;
np:hasProvenance
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_provenance
;
np:hasPublicationInfo
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_assertion
a
np:Assertion
.
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_provenance
a
np:Provenance
.
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_assertion
{
miriam-gene:55120
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNa6e51bcff8243f3e642234a922eb703f
sio:SIO_000628
miriam-gene:55120
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_provenance
{
dgn-np:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_assertion
dcterms:description
"[High concordance from independent studies by the Children's Cancer Group (CCG) and Pediatric Oncology Group (POG) associating favorable prognosis with combined trisomies 4, 10, and 17 in children with NCI Standard-Risk B-precursor Acute Lymphoblastic Leukemia: a Children's Oncology Group (COG) initiative.]. 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:15789069
;
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:NP461874.RA-XFiHGiNfbKDTPE4WlSXNaT3QtfdJ-7hUDn4zvpyoJA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}