@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM
> .
@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:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_head
{
this:
np:hasAssertion
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_assertion
;
np:hasProvenance
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_provenance
;
np:hasPublicationInfo
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_assertion
a
np:Assertion
.
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_provenance
a
np:Provenance
.
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN7ee7bfffb9a3a0b4b15c4ab4a1ffcef0
sio:SIO_000628
miriam-gene:7389
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_provenance
{
dgn-np:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_assertion
dcterms:description
"[Further studies of larger numbers of patients will be needed to determine whether 7q UPD detected by SNP array analysis will identify higher risk MDS patients at diagnosis, analogous to those with 7q cytogenetic abnormalities.]. 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:19387468
;
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:NP862666.RAqPkd5ZHI92E3n4jjfcDUS4tGTm2kZsvD3xSGVwq7fSM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}