@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y
> .
@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:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_head
{
this:
np:hasAssertion
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion
;
np:hasProvenance
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion
a
np:Assertion
.
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance
a
np:Provenance
.
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN2f765f98e72d15bb836c5373d8bc5a07
sio:SIO_000628
miriam-gene:4360
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_provenance
{
dgn-np:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_assertion
dcterms:description
"[We investigated 96 colorectal carcinomas, 58 gastric carcinomas and 41 endometrial carcinomas, occurring as part of inherited DNA mismatch repair (MMR) deficiency (Lynch syndrome), familial colorectal carcinoma without MMR gene mutations or sporadically.]. 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:21327300
;
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:NP173632.RAF2lSIRwvtkWay-B-0GlY2QJcCIO3ZhanG_VXSGLFx_Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}