@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848
> .
@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:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_head
{
this:
np:hasAssertion
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion
;
np:hasProvenance
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_provenance
;
np:hasPublicationInfo
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion
a
np:Assertion
.
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_provenance
a
np:Provenance
.
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1621958
a
ncit:C7057
.
dgn-gda:DGN18e57bdddfb2a1cddbf7bd5a9e682c40
sio:SIO_000628
miriam-gene:3342
,
lld:C1621958
;
a
sio:SIO_001121
.
}
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_provenance
{
dgn-np:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_assertion
dcterms:description
"[The present study compares the CGH evaluation of 22 GBM with classic cytogenetics, loss of heterozygosity by allelotyping, and gene amplification by Southern blot analysis to determine the reliability of CGH in the genetic characterization of GBM.]. 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:11302337
;
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:NP562966.RAioScwkGS5ukoetecT-PgCzwL9CEFTFRx28j7mu03848130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}