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http://rdf.disgenet.org/nanopublications.trig#NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY
> .
@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:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_head
{
this:
np:hasAssertion
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_assertion
;
np:hasProvenance
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_provenance
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np:hasPublicationInfo
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_assertion
a
np:Assertion
.
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_provenance
a
np:Provenance
.
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:4360
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGN0ee723c9c0b786e3b2de18862af2377d
sio:SIO_000628
miriam-gene:4360
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_provenance
{
dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_assertion
dcterms:description
"[In conclusion, our study shows that 1) IHC identifies a significant portion of colorectal tumors derived from MMR gene germline mutation carriers and can be used as an adjunct measure in the identification of HNPCC families, but IHC cannot replace MSI testing; 2) adenomas have similar MMR protein expression patterns as carcinomas and may serve as an adequate sample for screening purposes in the identification of patients with MMR mutations; 3) not all IHC-positive cases show uniform positivity throughout the tumor; and 4) weak and focal staining of an MMR protein may be associated with MSI or gene mutation or both, suggesting the need to incorporate staining intensity in further IHC studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:15613860
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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 .
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dgn-np:NP341096.RAWd4nxVBFK1h60Sw0wat_hjXcYRzzTi67VxqebMhFjPY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
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> ;
pav:version
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}