@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM
> .
@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:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_head
{
this:
np:hasAssertion
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_assertion
;
np:hasProvenance
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_assertion
a
np:Assertion
.
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_provenance
a
np:Provenance
.
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNb109090f49086be02ee6ec1509264363
sio:SIO_000628
miriam-gene:4360
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_provenance
{
dgn-np:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_assertion
dcterms:description
"[To explore whether loss of DNA mismatch repair (MMR) function is involved in AML, we screened two key MMR genes, MSH2 and MLH1, for mutations and promoter hypermethylation in leukemia specimens from 53 AML patients and blood from 17 non-cancer controls.]. 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:18227862
;
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:NP189532.RAxWBp6mDe_L85eICI4Rwsh8wzdJ9mYQ5ZrLSCawELYDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}