@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y
> .
@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:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_head
{
this:
np:hasAssertion
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_assertion
;
np:hasProvenance
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_assertion
a
np:Assertion
.
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_provenance
a
np:Provenance
.
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_assertion
{
miriam-gene:2623
a
ncit:C16612
.
lld:C0018939
a
ncit:C7057
.
dgn-gda:DGN7e0324c7a60890815cecd063da15221c
sio:SIO_000628
miriam-gene:2623
,
lld:C0018939
;
a
sio:SIO_001121
.
}
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_provenance
{
dgn-np:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_assertion
dcterms:description
"[Furthermore, few would have guessed that missense mutations in GATA1 would cause inherited blood disorders, while acquired mutations would be found associated with essentially all cases of acute megakaryoblastic leukemia (AMKL) in children with Down syndrome (DS).]. 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:15659348
;
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:NP858008.RAItXBPMbGqHcdaH0v9D4vWVCj083Ko7_wJSaRekeBh_Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}