@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0
> .
@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:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_head
{
this:
np:hasAssertion
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_assertion
;
np:hasProvenance
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_provenance
;
np:hasPublicationInfo
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_assertion
a
np:Assertion
.
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_provenance
a
np:Provenance
.
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN037758faf6c2ab6eb59ea2639be78e70
sio:SIO_000628
miriam-gene:4292
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_provenance
{
dgn-np:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_assertion
dcterms:description
"[These data imply that relatives of CRC cases with MLH1 methylation may be at increased risk of CRC and stomach cancer and possibly ovarian and liver cancer, suggesting that there may be a heritable factor for CRC and other cancers associated with MLH1 methylation in non-Lynch syndrome CRCs.]. 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:22144422
;
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:NP306319.RAERcoQrSo12DF5SgyDNDTN5OtU7wyf7DLkJYIVZ9ypa0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}