@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA
> .
@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:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_head
{
this:
np:hasAssertion
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion
;
np:hasProvenance
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion
a
np:Assertion
.
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance
a
np:Provenance
.
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN3c5ef13610a3b4c45f4c227daa71504e
sio:SIO_000628
miriam-gene:4360
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_provenance
{
dgn-np:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_assertion
dcterms:description
"[We examined the validity of immunohistochemistry for mismatch repair (MMR) proteins in colorectal cancer specimens to identify patients at risk for Lynch syndrome (hereditary nonpolyposis colorectal cancer) and patients with sporadic microsatellite instable colorectal cancer.]. 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:18677806
;
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:NP182238.RACnBqtpXtAR8OVsR0lPwcjVFCTFBNXSONmzYm-2zteaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}