@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA
> .
@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:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_head
{
this:
np:hasAssertion
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion
;
np:hasProvenance
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion
a
np:Assertion
.
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance
a
np:Provenance
.
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion
{
miriam-gene:140738
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8c9443153b60697dd468c319309ed502
sio:SIO_000628
miriam-gene:140738
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_provenance
{
dgn-np:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_assertion
dcterms:description
"[Conventional cytogenetic study of TSU-PR1 showed aneuploidy, ranging from 65 to 86 chromosome with a modal number of 80, and with 10 marker chromosomes, thus conventional cytogenetics cannot be used to determine which chromosomes or regions of chromosomes are critical in cancer development and progression of this cell line.]. 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:16271951
;
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:NP841736.RAHfVoyiwuFY0KQznOaTJreFcaH8NJjiv3XeZatDGdWyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}