@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw
> .
@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:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion
a
np:Assertion
.
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_provenance
a
np:Provenance
.
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo
a
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.
}
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN0d4f2393a115541f94bdbc40b182e17b
sio:SIO_000628
miriam-gene:4360
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_provenance
{
dgn-np:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_assertion
dcterms:description
"[We found no evidence that the SNPs associated with CRC in the general population are modifiers of the risk for MMR gene mutation carriers overall, and therefore any evidence of proven clinical utility in Lynch syndrome.]. 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:23434150
;
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:NP1055225.RAapIPwOURgzlMRDWS8fp_HIARL5mYyCLBDtbaFQCEjCw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:44+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
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;
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" .
}