@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E
> .
@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:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_head
{
this:
np:hasAssertion
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_assertion
;
np:hasProvenance
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_provenance
;
np:hasPublicationInfo
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_assertion
a
np:Assertion
.
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_provenance
a
np:Provenance
.
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN11fbd96607b6627f0bce81f87d5b1e57
sio:SIO_000628
miriam-gene:5728
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_provenance
{
dgn-np:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_assertion
dcterms:description
"[This is the first report on CRC in Malaysia showing comparable frequency of KRAS mutation and PTEN loss, lower BRAF mutation rate, higher PIK3CA amplification frequency, and rare PTEN mutation, as compared with published reports.]. 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:23992303
;
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:NP185793.RACvj8HTTFDZx884MjeS3yvdsTL8PSe1VDf_3INaks94E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}