@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M
> .
@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:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_head
{
this:
np:hasAssertion
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion
;
np:hasProvenance
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance
;
np:hasPublicationInfo
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion
a
np:Assertion
.
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance
a
np:Provenance
.
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN593cb8b9a3d4bc81cd06679ea5884387
sio:SIO_000628
miriam-gene:4292
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_provenance
{
dgn-np:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_assertion
dcterms:description
"[Four of the 28 MSI-H cases, including one Amsterdam criteria case, had biallelic tumor MLH1 methylation, indicating that sporadic cases can be admixed in with Lynch syndrome cases, even those meeting the strongest criteria for Lynch syndrome.]. 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:19690142
;
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:NP758260.RABKtASL1pAIUgmVWaUO1rkiLOXLxFeGQulsf4au7h91M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:28+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" .
}