@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo
> .
@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:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_head
{
this:
np:hasAssertion
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion
;
np:hasProvenance
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance
;
np:hasPublicationInfo
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion
a
np:Assertion
.
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance
a
np:Provenance
.
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0342494
a
ncit:C7057
.
dgn-gda:DGN9fe93413dcbe66144a332f316580fc27
sio:SIO_000628
miriam-gene:1029
,
lld:C0342494
;
a
sio:SIO_001121
.
}
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_provenance
{
dgn-np:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_assertion
dcterms:description
"[Differentiation between benign and malignant tumors of the adrenal cortex was attempted by microdissection of nine cases of adrenal cortical hyperplasia, 10 cortical adenomas, and 18 adrenal cortical carcinomas with subsequent polymerase chain reaction (PCR) amplification for loss of heterozygosity (LOH) of five microsatellites of putative tumor suppressor gene loci: p53 gene (17p), the neuroblastoma candidate gene (1p), the p16 gene (9p), the von Hippel Lindau gene (3p), and the retinoblastoma gene (13q).]. 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:9596277
;
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:NP205835.RAbmepN9A2QUiDN5oGKhEEaQz17Xh8s9W-MClf3TqIUuo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}