@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew
> .
@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:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_head
{
this:
np:hasAssertion
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_assertion
;
np:hasProvenance
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_provenance
;
np:hasPublicationInfo
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_assertion
a
np:Assertion
.
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_provenance
a
np:Provenance
.
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGNc408e782b7d2d6613f41828f4f9d1db6
sio:SIO_000628
miriam-gene:4360
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_provenance
{
dgn-np:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_assertion
dcterms:description
"[Circumstantial evidence suggests that the MMR defect may be involved in some lymphoid malignancies, although several allelotype analyses have concluded on the low level of microsatellite instability in acute lymphoblastic leukemias.]. 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:9639521
;
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:NP561486.RA-18ll1jUheb1R3zjBgRNae0cc9lA0Yp_zVhDFtDL-ew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}