@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_head
{
this:
np:hasAssertion
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_assertion
;
np:hasProvenance
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_provenance
;
np:hasPublicationInfo
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_assertion
a
np:Assertion
.
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_provenance
a
np:Provenance
.
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN2d8c0da3905a84e867ffcf44640aded7
sio:SIO_000628
miriam-gene:4360
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_provenance
{
dgn-np:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_assertion
dcterms:description
"[Carcinomas of the small intestine are rare, but the risk is greatly increased in patients with hereditary nonpolyposis colorectal cancer (HNPCC) due to an inherited mismatch repair (MMR) gene mutation, most commonly affecting the genes MLH1 or MSH2.]. 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:12627520
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP404437.RAQ6-Idm7-T_eNEWHnEnI-qrKmExy3koRugJxMzGwTYtw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}