@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE
> .
@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:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_head
{
this:
np:hasAssertion
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_assertion
;
np:hasProvenance
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_assertion
a
np:Assertion
.
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_provenance
a
np:Provenance
.
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0585215
a
ncit:C7057
.
dgn-gda:DGN72c1b11f6d4251ca0873e9b01338989b
sio:SIO_000628
miriam-gene:2187
,
lld:C0585215
;
a
sio:SIO_001121
.
}
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_provenance
{
dgn-np:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_assertion
dcterms:description
"[Modification of the FAB system to incorporate additional diagnostic features such as pretreatment fetal hemoglobin (Hb F) and cytogenetics allowed incorporation of the categories of juvenile chronic myeloid leukemia (JCML) and infantile monosomy 7 syndrome (IMo7).]. 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:7703482
;
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:NP660651.RAHUS2veygFVzhv6wUE5IhwexI7TOjOnViw7HKquy8xGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}