@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI
> .
@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:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_head
{
this:
np:hasAssertion
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_assertion
;
np:hasProvenance
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_provenance
;
np:hasPublicationInfo
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_assertion
a
np:Assertion
.
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_provenance
a
np:Provenance
.
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0280100
a
ncit:C7057
.
dgn-gda:DGN3cbe0f138047763ef40d7215c25945e1
sio:SIO_000628
miriam-gene:3342
,
lld:C0280100
;
a
sio:SIO_001121
.
}
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_provenance
{
dgn-np:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_assertion
dcterms:description
"[Therefore, this simplified CGH technique is suitable for routine screening of pediatric solid tumors for amplifications when genetic studies are important but sample sizes are small and dividing cells are infrequent or unavailable.]. 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:8705194
;
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:NP266578.RAe7iEtmU5W-82U_Cwfoz8oKkG9P8mfKG2KqW0ZhSQokI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}