@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM
> .
@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:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_head
{
this:
np:hasAssertion
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_assertion
;
np:hasProvenance
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_assertion
a
np:Assertion
.
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_provenance
a
np:Provenance
.
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN774bae7682df5e047452dde2bfca799b
sio:SIO_000628
miriam-gene:2064
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_provenance
{
dgn-np:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_assertion
dcterms:description
"[The purpose of this study was to use the fluorescence in situ hybridization (FISH) technique for the assessment of ERBB2 and MYC amplification and TP53 deletion, and to relate these molecular markers to clinical and pathologic factors in Saudi patients with hepatocellular carcinoma.]. 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:21156243
;
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:NP678283.RA_G1wGr12gYrOi3bjk8ITfcsV19J0MyGJqCv6HScvzjM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}