@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY
> .
@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:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_head
{
this:
np:hasAssertion
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_assertion
;
np:hasProvenance
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_assertion
a
np:Assertion
.
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_provenance
a
np:Provenance
.
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C1860787
a
ncit:C7057
.
dgn-gda:DGN1d7a8881d32d945d32fbe49cfa1a5277
sio:SIO_000628
miriam-gene:861
,
lld:C1860787
;
a
sio:SIO_001121
.
}
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_provenance
{
dgn-np:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_assertion
dcterms:description
"[Fluorescence in situ hybridization analyses of the ring showed one chromosome 21 centromere, two copies each of the AML1 gene (q22) and the Down syndrome critical region, and deleted subtelomeric material.]. 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:16155419
;
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:NP836380.RAkNkxQPfSq2hxBuFSi6z80MJgaRzOz9cUqbursCWeRaY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}