@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s
> .
@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:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_head
{
this:
np:hasAssertion
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_assertion
;
np:hasProvenance
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_provenance
;
np:hasPublicationInfo
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_assertion
a
np:Assertion
.
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_provenance
a
np:Provenance
.
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_assertion
{
miriam-gene:6287
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN193d2f9c1d7b30d0a2bfc289802a0e69
sio:SIO_000628
miriam-gene:6287
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_provenance
{
dgn-np:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_assertion
dcterms:description
"[SAA and hypoplastic MDS (HMDS) are discussed in the light of these findings and attempts to separate nonevolving bone marrow failure syndromes from marrow failure progressing to acute leukemia are reviewed.]. 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:10676908
;
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:NP777017.RAdSM924OQlvPHf3unc5kyoZbkHqOXwsOuaDAk94Oxd6s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}