@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4
> .
@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:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_head
{
this:
np:hasAssertion
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_assertion
;
np:hasProvenance
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_provenance
;
np:hasPublicationInfo
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_assertion
a
np:Assertion
.
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_provenance
a
np:Provenance
.
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN9ba2213015424bc51de2cc28b782f28f
sio:SIO_000628
miriam-gene:4360
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_provenance
{
dgn-np:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_assertion
dcterms:description
"[We showed earlier that routine screening for microsatellite instability (MSI) and loss of mismatch repair (MMR) protein expression in colorectal cancer (CRC) led to the identification of previously unrecognized cases of Lynch syndrome (LS).]. 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:24474394
;
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:NP1149911.RAbAu9AD3v0xX_RtWxFtFFer2vyQxQh013YCPWNa6jqA4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:27+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" .
}