@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ
> .
@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:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_head
{
this:
np:hasAssertion
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_assertion
;
np:hasProvenance
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_assertion
a
np:Assertion
.
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_provenance
a
np:Provenance
.
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_assertion
{
miriam-gene:3090
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNeb712a56849bcc55fb012495b7182782
sio:SIO_000628
miriam-gene:3090
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_provenance
{
dgn-np:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_assertion
dcterms:description
"[The aim of this study was to investigate the methylation of the SFRP2, P16, DAPK1, HIC1, and MGMT genes, as well as the mutation of amino acid codons 12 and 13 of the KRAS gene in normal and tumor tissue DNA of patients diagnosed with sporadic colorectal cancer (SCRC).]. 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:20682398
;
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:NP426105.RAzl8kjIbUVDBzHRWNUwOui8p3o2gZOG7VSf8pSAoPBoQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}