@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y
> .
@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:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_head
{
this:
np:hasAssertion
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_assertion
;
np:hasProvenance
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_assertion
a
np:Assertion
.
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_provenance
a
np:Provenance
.
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN3d90ae093ae00c08ebf66f2360c8d0bd
sio:SIO_000628
miriam-gene:673
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_provenance
{
dgn-np:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_assertion
dcterms:description
"[To evaluate our experience of adding reflex BRAF mutation analysis following mismatch repair (MMR) protein staining in the test algorithm for Lynch syndrome (LS), the most common inherited predisposition to colorectal cancer (CRC).]. 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:23897252
;
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:NP1097920.RApJTbajUTLsAZBQSVLH17Kj7k8X9s3llLbdxpY5LmN5Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:03+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:disgenetv3.0rdf
;
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" .
}