@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y
> .
@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:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_head
{
this:
np:hasAssertion
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_assertion
;
np:hasProvenance
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_assertion
a
np:Assertion
.
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_provenance
a
np:Provenance
.
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_assertion
{
miriam-gene:2120
a
ncit:C16612
.
lld:C1636667
a
ncit:C7057
.
dgn-gda:DGN09b1ac10042d223c57c504205c3ceec0
sio:SIO_000628
miriam-gene:2120
,
lld:C1636667
;
a
sio:SIO_001121
.
}
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_provenance
{
dgn-np:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_assertion
dcterms:description
"[Clinicohematological data in these studies as well as the restriction mapping of chromosomal breakpoints strongly suggest that (1) common features in MDSs involving the TEL gene are monocytosis and eosinophilia, (2) chromosomes other than no.]. 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:7742547
;
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:NP666618.RAK-galVvTgGK0C0Pr2NfXxBlBITyEldX6gQXO5Ymco0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}