@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc
> .
@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:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_head
{
this:
np:hasAssertion
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_assertion
;
np:hasProvenance
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_provenance
;
np:hasPublicationInfo
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_assertion
a
np:Assertion
.
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_provenance
a
np:Provenance
.
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_assertion
{
miriam-gene:2048
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGN34ce893c0aae1b4d3215eea04a97a080
sio:SIO_000628
miriam-gene:2048
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_provenance
{
dgn-np:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_assertion
dcterms:description
"[A search was made for mutations at the A9 tract in exon 17, an allelic loss at the EPHB2 gene locus, and promoter hypermethylation of the EPHB2 gene in 81 sporadic gastric cancers in order to determine if genetic or epigenetic alterations of the EPHB2 gene are involved in the development and/or progression of gastric cancer.]. 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:17295683
;
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:NP926821.RAekpSyZqSx4AsV49xsfEPAPKCYg0gH8o660I2Ykq9ILc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}