@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A
> .
@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:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_head
{
this:
np:hasAssertion
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_assertion
;
np:hasProvenance
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_provenance
;
np:hasPublicationInfo
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_assertion
a
np:Assertion
.
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_provenance
a
np:Provenance
.
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN17167e0218c0d9b1f74381447e6b894f
sio:SIO_000628
miriam-gene:4292
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_provenance
{
dgn-np:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_assertion
dcterms:description
"[The Lynch syndrome (LS) is an inherited cancer syndrome showing a preponderance of colorectal cancer (CRC) in context with endometrial cancer and several other extracolonic cancers, which is due to pathogenic mutations in the mismatch repair (MMR) genes, MLH1, MSH2, MSH6, and PMS2.]. 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:21769135
;
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:NP910700.RA2cIE8AfEcBlk_DPcz3YVK0o6EMV27FMNC1X72GRnH0A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:36+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" .
}