@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_head
{
this:
np:hasAssertion
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_assertion
;
np:hasProvenance
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_provenance
;
np:hasPublicationInfo
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_assertion
a
np:Assertion
.
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_provenance
a
np:Provenance
.
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0024305
a
ncit:C7057
.
dgn-gda:DGN2b028cf48df3f498a68d3d2a7139f637
sio:SIO_000628
miriam-gene:4436
,
lld:C0024305
;
a
sio:SIO_001122
.
}
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_provenance
{
dgn-np:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_assertion
dcterms:description
"[Twenty-two individuals with non-Hodgkin lymphomas (NHL) and 50 normal individuals were screened for polymorphic variants in exon 13 of the hMSH2 mismatch repair gene in order to determine if there is any association with development of lymphomas.]. 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:11890986
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP73350.RAt_2cUwOlXFlk0HQOyhSu0VexEqXjWFic5yM-AAZFP9E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:21+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}