@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg
> .
@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:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_head
{
this:
np:hasAssertion
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_assertion
;
np:hasProvenance
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_assertion
a
np:Assertion
.
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_provenance
a
np:Provenance
.
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0007130
a
ncit:C7057
.
dgn-gda:DGNa85da00dafeba558dbde7098f647e53a
sio:SIO_000628
miriam-gene:4360
,
lld:C0007130
;
a
sio:SIO_001121
.
}
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_provenance
{
dgn-np:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_assertion
dcterms:description
"[Although some phenotypes (eg, mucinous adenocarcinoma) have been shown to be associated with deficient mismatch repair (MMR) and thus microsatellite instability (MSI), the MMR protein status of colorectal SCNCs has not been investigated.]. 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:17063080
;
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:NP795099.RAhslliENs3i_lJN5RCpiJYGUBiSjaBXnqHvuDlQIdlVg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}