@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI
> .
@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:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_head
{
this:
np:hasAssertion
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_assertion
;
np:hasProvenance
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_provenance
;
np:hasPublicationInfo
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_assertion
a
np:Assertion
.
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_provenance
a
np:Provenance
.
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_assertion
{
miriam-gene:673
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN58572427423d29d9729998e2f3b6021c
sio:SIO_000628
miriam-gene:673
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_provenance
{
dgn-np:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_assertion
dcterms:description
"[The identification of Lynch syndrome has been greatly assisted by the advent of tumour immunohistochemistry (IHC) for mismatch repair (MMR) proteins, and by the recognition of the role of acquired somatic BRAF mutation in sporadic MMR-deficient 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:19241144
;
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:NP223259.RACWfBvY3C1BDzexY-ueQWQpzF1ucQNrl86tKzPEK8NFI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:04+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" .
}