@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU
> .
@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:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_head
{
this:
np:hasAssertion
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_assertion
;
np:hasProvenance
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_provenance
;
np:hasPublicationInfo
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_assertion
a
np:Assertion
.
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_provenance
a
np:Provenance
.
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_assertion
{
miriam-gene:7301
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGNde773d5ea746dd427106b33813f89a34
sio:SIO_000628
miriam-gene:7301
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_provenance
{
dgn-np:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_assertion
dcterms:description
"[The SKY has been applied to various tumor groups including hematological malignancies, sarcomas, carcinomas and brain tumors, with the intent of identifying specific chromosomal abnormalities that may provide insight to the genes involved in the disease process as well as identifying recurrent cytogenetic markers for clinical diagnosis and prognostic assessment.]. 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:12025233
;
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:NP903491.RADaOg_Kyl1IGHAYbgU3DgDa-grDYTZnIjv6LZyjGilaU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}