@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw
> .
@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:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_head
{
this:
np:hasAssertion
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_assertion
;
np:hasProvenance
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_provenance
;
np:hasPublicationInfo
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_assertion
a
np:Assertion
.
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_provenance
a
np:Provenance
.
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGNf35b42cef596213ffaaefc5a55ff51a0
sio:SIO_000628
miriam-gene:3845
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_provenance
{
dgn-np:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_assertion
dcterms:description
"[Integration of information on the genetic and epigenetic alterations revealed that the GCs with the CpG island methylator phenotype (CIMP) tended to have mutations of oncogenes, CTNNB1, ERBB2, KRAS, and PIK3CA.]. 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:23196062
;
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:NP746382.RAaGk_A9VhF0VLCoqnQEJhA2PK-S7wL-iGM3QqtSgaKbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+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" .
}