@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_head
{
this:
np:hasAssertion
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion
;
np:hasProvenance
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion
a
np:Assertion
.
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance
a
np:Provenance
.
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN65cd0e6a00376b7d42322a182da5c994
sio:SIO_000628
miriam-gene:5728
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_provenance
{
dgn-np:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1106683.RAtvIQ7k0-60idqd7I833sSNboSyAP120_oVbKMIAE1EQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:07+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}