@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78
> .
@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:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_head
{
this:
np:hasAssertion
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_assertion
;
np:hasProvenance
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_provenance
;
np:hasPublicationInfo
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_assertion
a
np:Assertion
.
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_provenance
a
np:Provenance
.
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_assertion
{
miriam-gene:57026
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGN9edb672d907904bb58def518ba5c6da9
sio:SIO_000628
miriam-gene:57026
,
lld:C0009404
;
a
sio:SIO_001121
.
}
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_provenance
{
dgn-np:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_assertion
dcterms:description
"[As MSI(+) tumors appear to form a unique clinicopathological and molecular entity that is clearly distinct from that of classical colorectal tumors, which are accompanied by chromosomal instability (CIN), an exclusive pathway of tumorigenesis has been proposed in 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:16341479
;
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:NP351234.RAgg08kyMybIwJCgSZvpK0k8OdCAJHFdcwZcpEgxrg_78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}