@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY
> .
@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:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_head
{
this:
np:hasAssertion
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_assertion
;
np:hasProvenance
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_provenance
;
np:hasPublicationInfo
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_assertion
a
np:Assertion
.
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_provenance
a
np:Provenance
.
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN57639573dfce5876d2dff132953bd7a8
sio:SIO_000628
miriam-gene:7248
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_provenance
{
dgn-np:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_assertion
dcterms:description
"[The occurrence of retinoblastoma gene abnormalities in a large subset of various malignancies suggests an important role for this tumour suppressor gene in carcinogenesis, but this varies considerably from one tumour type to another and results in patients with acute myeloid leukaemia (AML) have been controversial.]. 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:8759895
;
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:NP182156.RAMldEPNKtpL6FNS63clNbVzJwEjak0EjPKTaU1bgm-MY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}