@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo
> .
@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:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_head
{
this:
np:hasAssertion
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion
;
np:hasProvenance
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance
;
np:hasPublicationInfo
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion
a
np:Assertion
.
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance
a
np:Provenance
.
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN62e1cc25f6a08f96ba0fb3bc2709d3ff
sio:SIO_000628
miriam-gene:5925
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_provenance
{
dgn-np:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_assertion
dcterms:description
"[In order to address a possible role for the human retinoblastoma susceptibility (RB1) gene in hematopoietic malignancies, 34 cases of different types of leukemia without chromosomal abnormalities at band 13q14 were analyzed by Southern blot hybridization.]. 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:1884351
;
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:NP550816.RATltRf9mnulQOKLBleBwBr4jVSHR8Y88TDzwpjK5IZWo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}