@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8
> .
@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:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_head
{
this:
np:hasAssertion
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion
;
np:hasProvenance
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion
a
np:Assertion
.
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance
a
np:Provenance
.
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0024623
a
ncit:C7057
.
dgn-gda:DGN51bcfd0ba6c8894ce9355958a2d65ef1
sio:SIO_000628
miriam-gene:5290
,
lld:C0024623
;
a
sio:SIO_001121
.
}
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance
{
dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_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:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}