@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8
> .
@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:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_head
{
this:
np:hasAssertion
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion
a
np:Assertion
.
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_provenance
a
np:Provenance
.
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4292
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGN053eeba58163ebf015deb8370db0bcad
sio:SIO_000628
miriam-gene:4292
,
lld:C0009404
;
a
sio:SIO_001121
.
}
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_provenance
{
dgn-np:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_assertion
dcterms:description
"[We investigated the clinical and molecular features of the MSH6 variants, such as the family cancer history, pathological findings, immunohistochemistry, methylation status of the MLH1 promoter and BRAF mutation in the colorectal tumor.]. 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:24100870
;
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:NP1116973.RAqEmxEc5aJ5Cc99FCCip-cCnwhN9WwgXrefcVF-QI6x8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:12+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
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;
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" .
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"v4.0.0" .
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