@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA
> .
@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:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_head
{
this:
np:hasAssertion
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_assertion
;
np:hasProvenance
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_provenance
;
np:hasPublicationInfo
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_assertion
a
np:Assertion
.
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_provenance
a
np:Provenance
.
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_assertion
{
miriam-gene:4507
a
ncit:C16612
.
lld:C0149676
a
ncit:C7057
.
dgn-gda:DGN6edc5801453d04efdf24d96e3fac80af
sio:SIO_000628
miriam-gene:4507
,
lld:C0149676
;
a
sio:SIO_001121
.
}
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_provenance
{
dgn-np:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_assertion
dcterms:description
"[These findings indicate that loss of chromosomal material in the region of 9p21-p22 is closely associated with lymphomatous ALL; by analogy with retinoblastoma, in which gene deletions are associated with an enzyme deficiency, this disease may be related to the loss of the enzyme methylthioadenosine phosphorylase, previously reported in some of these patients.]. 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:3925340
;
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:NP487717.RAOX4ewr_tzpnnLzquvJdSixWfBra_jIZdJX8l7IPB3VA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}