@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8
> .
@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:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_head
{
this:
np:hasAssertion
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_assertion
;
np:hasProvenance
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_provenance
;
np:hasPublicationInfo
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_assertion
a
np:Assertion
.
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_provenance
a
np:Provenance
.
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_assertion
{
miriam-gene:4680
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN4414039f5827da9b9d7f3ea329f4345f
sio:SIO_000628
miriam-gene:4680
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_provenance
{
dgn-np:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_assertion
dcterms:description
"[The feasibility of detecting numerical chromosomal abnormalities (NCA) in malignant cells on fine needle aspirates (FNA) using the fluorescent in situ hybridization (FISH) technique was tested on clinical specimens from patients with various neoplasms.]. 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:8388611
;
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:NP800915.RAEslI42XYJ7NoKCEJ_6y87r2a5zy_577LHSihUhkWVq8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}