@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM
> .
@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:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_head
{
this:
np:hasAssertion
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion
;
np:hasProvenance
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance
;
np:hasPublicationInfo
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion
a
np:Assertion
.
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance
a
np:Provenance
.
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion
{
miriam-gene:338386
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8ad0c5573c50428db59048c196e23ee4
sio:SIO_000628
miriam-gene:338386
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_provenance
{
dgn-np:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_assertion
dcterms:description
"[These findings suggest that: (a) the amplification produces c-erbB-2 in the HSR form generally early in the carcinogenesis of gastric adenocarcinomas; and (b) in the process of cancer development, the amplified gene is lost in some cancer cells by uneven segregation of HSR in mitosis, whereas in others, it is kept in HSR or translocated to other chromosomal positions, thereby preserving overexpression of c-erbB-2 protein.]. 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:9520947
;
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:NP690486.RAssZtxjyVO06kuQaHaSWYvkHl1K9Gu2Er4D073J0JayM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}