@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_head
{
this:
np:hasAssertion
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_assertion
;
np:hasProvenance
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_assertion
a
np:Assertion
.
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_provenance
a
np:Provenance
.
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_assertion
{
miriam-gene:2098
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGNef65c17cb3fd6bc89c1e0665a4980901
sio:SIO_000628
miriam-gene:2098
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_provenance
{
dgn-np:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_assertion
dcterms:description
"[However, it was recognition of both the deletion of band q14 of chromosome 13 in mentally retarded children with retinoblastoma, and the linkage of retinoblastoma with the genetic marker esterase D, which resulted in the eventual cloning of the gene.]. 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:2227145
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP955518.RACXhDAxC1Nr51t9OKaVSdLgP2s5cTwy0oZKwoZ3KNT8o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:58+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}