@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc
> .
@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:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_head
{
this:
np:hasAssertion
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion
;
np:hasProvenance
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance
;
np:hasPublicationInfo
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion
a
np:Assertion
.
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance
a
np:Provenance
.
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion
{
miriam-gene:9212
a
ncit:C16612
.
lld:C1623038
a
ncit:C7057
.
dgn-gda:DGN5ca686642489fbb432ec50a29c14631a
sio:SIO_000628
miriam-gene:9212
,
lld:C1623038
;
a
sio:SIO_001121
.
}
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_provenance
{
dgn-np:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_assertion
dcterms:description
"[The expression of Aurora B and splicing variant forms were screened in 125 HCC patients (94 chronic hepatitis with cirrhosis background liver specimens), 18 metastatic liver cancer patients and 16 normal liver specimens by cDNA microarray, reverse transcription -- polymerase chain reaction (RT-PCR) and Real time quantitative Reverse Transcription PCR (qRT-PCR).]. 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:19134008
;
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:NP651431.RA0cmQ3qI71z71m4FEdBBr-WRMrP9EK0xE8Bpbjz2uabc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:32+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" .
}