@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw
> .
@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:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_head
{
this:
np:hasAssertion
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_assertion
;
np:hasProvenance
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_provenance
;
np:hasPublicationInfo
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_assertion
a
np:Assertion
.
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_provenance
a
np:Provenance
.
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGN9e7c205fedb74bdc21c29df2533438f0
sio:SIO_000628
miriam-gene:4436
,
lld:C0009404
;
a
sio:SIO_001121
.
}
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_provenance
{
dgn-np:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_assertion
dcterms:description
"[MSH2 is one of the genes involved in DNA mismatch repair to maintain fidelity of genomic replication, and defects of MSH2 are directly involved in MSI in hereditary nonpolyposis colorectal tumors and other human tumors.]. 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:10397740
;
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:NP650575.RA9eh8jRS9zATuORI7BRu78JBePjsy4dAzvm3OskK-YXw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}