@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8
> .
@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:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_head
{
this:
np:hasAssertion
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion
;
np:hasProvenance
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion
a
np:Assertion
.
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance
a
np:Provenance
.
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion
{
miriam-gene:8996
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNa7451fb81f0848b825364a968ed103fa
sio:SIO_000628
miriam-gene:8996
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_provenance
{
dgn-np:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_assertion
dcterms:description
"[While our results suggest that interactive IA is potentially a more sensitive method than FCM for detecting aneuploidy in cutaneous pigmented lesions, it remains to be shown whether this will translate into better prognostic assessment of the biologic behavior of melanocytic neoplasms than provided by flow cytometric ploidy analysis.]. 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:1558616
;
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:NP900699.RA9AGml2X0NgJT1emCgF2y9_ytalIFarvuxxnakiWVrE8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}