@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo
> .
@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:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_head
{
this:
np:hasAssertion
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_assertion
;
np:hasProvenance
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_provenance
;
np:hasPublicationInfo
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_assertion
a
np:Assertion
.
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_provenance
a
np:Provenance
.
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_assertion
{
miriam-gene:3456
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN4b86cd6403dc05c08809dc6159ba862c
sio:SIO_000628
miriam-gene:3456
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_provenance
{
dgn-np:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_assertion
dcterms:description
"[Our results reveal the following: (a) for those cases in which loss has occurred, the region of common loss lies on the short (p) arm of the chromosome; (b) loss of genetic information from the short arm of chromosome 9 occurs frequently in glial tumors of intermediate (anaplastic, grade III) and high (glioblastoma, grade IV) histological malignancy (10 of 20 cases) but not in tumors of low (grade II) histological malignancy (0 of 10 cases); (c) tumors with 9p deletions are hemi- or nullizygous for interferon beta-1 and the interferon alpha gene cluster; (d) cases of interferon nullizygosity occur exclusively among tumors of highest histological malignancy (glioblastoma).]. 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:1998958
;
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:NP437028.RA517p2DJvXuomuSMBlXgf9b-7jxlBxOueeZRGZPL-Clo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}