@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04
> .
@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:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_head
{
this:
np:hasAssertion
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_assertion
;
np:hasProvenance
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_provenance
;
np:hasPublicationInfo
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_assertion
a
np:Assertion
.
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_provenance
a
np:Provenance
.
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_assertion
{
miriam-gene:4597
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNee8a2aafa94874d86199af2ca95630e9
sio:SIO_000628
miriam-gene:4597
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_provenance
{
dgn-np:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_assertion
dcterms:description
"[Clonal disorders of hematopoiesis, such as myelodysplastic syndromes (MDS) and myeloproliferative diseases (MPD), affect both hematopoietic stem cells and progenitor cells within the erythroid, platelet and granulocytic lineages and can have devastating consequences in children and adults.]. 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:16304374
;
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:NP533663.RAf_Fv5NGG8sIr9q6KhfXe5NV9Zi9TMES0FdFza6Id_04130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}