@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I
> .
@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:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_head
{
this:
np:hasAssertion
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_assertion
;
np:hasProvenance
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_provenance
;
np:hasPublicationInfo
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_assertion
a
np:Assertion
.
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_provenance
a
np:Provenance
.
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN2b18ed37b074e50bdba11a6bac417861
sio:SIO_000628
miriam-gene:4360
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_provenance
{
dgn-np:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_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:NP1097916.RAto9aTUYMrs66dib-cDecMWEgVQ7r2aELld5Hc3gWD9I130_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" .
}