@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8
> .
@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:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_head
{
this:
np:hasAssertion
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_assertion
;
np:hasProvenance
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_provenance
;
np:hasPublicationInfo
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_assertion
a
np:Assertion
.
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_provenance
a
np:Provenance
.
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN3424fac6e7c9bda3fe3a1fa579589e86
sio:SIO_000628
miriam-gene:64127
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_provenance
{
dgn-np:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_assertion
dcterms:description
"[36 patients operated on for colon cancer, with familiar prevalence of this malignancy, were investigated using the DNA microarrays method with the potential detection of 170 mutations in MLH1, MSH2, MSH6, CHEK2, and NOD2 genes.]. 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:23741719
;
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:NP812651.RAf7-J89mej3fPe-wurrfJ13SM7lK6wN8VJHkSVElCLP8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:18+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" .
}