@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_head
{
this:
np:hasAssertion
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion
;
np:hasProvenance
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance
;
np:hasPublicationInfo
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion
a
np:Assertion
.
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance
a
np:Provenance
.
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C2939461
a
ncit:C7057
.
dgn-gda:DGN45dab556ebd733db0accf88809983ad4
sio:SIO_000628
miriam-gene:861
,
lld:C2939461
;
a
sio:SIO_001121
.
}
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_provenance
{
dgn-np:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_assertion
dcterms:description
"[Abstract Familial platelet disorder with predisposition to acute myeloid leukemia (FPD/AML) is an autosomal dominant disorder characterized by mild to moderate thrombocytopenia with or without its impaired function, inherited RUNX1 mutation and high incidence of myeloid malignancy, such as myelodysplastic syndrome or acute myeloid leukemia.]. 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:23971860
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP285479.RA7HV9u55AX8OtBAjom-8ip6WBmpX2aQdXHMb8y7kV6GY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:23+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}