@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8
> .
@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:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_head
{
this:
np:hasAssertion
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_assertion
;
np:hasProvenance
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_provenance
;
np:hasPublicationInfo
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_assertion
a
np:Assertion
.
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_provenance
a
np:Provenance
.
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN9b47555eaf6cc8e474390ce4a616ef5b
sio:SIO_000628
miriam-gene:4292
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_provenance
{
dgn-np:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_assertion
dcterms:description
"[Germline inactivation of MMR genes (hMLH1, hMSH2, hMSH6, and hPMS2) underlies the hereditary CRC with MMR defect (Lynch syndrome) and epigenetic silencing of hMLH1 gene causes the sporadic CRC with MMR defect.]. 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:15528793
;
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:NP467682.RAa5th0PvV351ys-iwjFxNv9ZlXPMpgVVD1bKL9Rp-Js8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:16+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" .
}