@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s
> .
@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:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_head
{
this:
np:hasAssertion
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_assertion
;
np:hasProvenance
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_assertion
a
np:Assertion
.
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_provenance
a
np:Provenance
.
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_assertion
{
miriam-gene:8996
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN6424cb27c3c1e9950223704c3aed9dda
sio:SIO_000628
miriam-gene:8996
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_provenance
{
dgn-np:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_assertion
dcterms:description
"[A total of 71 cases of pleural effusion in patients with and without cancer were analyzed by conventional cytology and flow cytometry (FCM) in order to detect cells with an abnormal DNA content (aneuploidy).]. 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:1296045
;
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:NP237837.RAT410tgbhRy-Hs_K9f3Vv5Ecr81F_JqFHGljOr-jps5s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}