@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A
> .
@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:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_head
{
this:
np:hasAssertion
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_assertion
;
np:hasProvenance
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_assertion
a
np:Assertion
.
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_provenance
a
np:Provenance
.
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNaf5ee888078d96355f66dc1f0f103eb7
sio:SIO_000628
miriam-gene:4360
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_provenance
{
dgn-np:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_assertion
dcterms:description
"[Unlike microsatellite unstable CRCs where hypermethylation of the DNA mismatch repair (MMR) gene hMLH1's promoter is causal, the precise cause of EMAST is not clearly defined but points towards hMSH3 deficiency.]. 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:23226332
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1034851.RAwLwau58wZ8r4h0LB9-1ltx3NWarJjOq1xz6vRyDKK8A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:35+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: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" .
}