@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM
> .
@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:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_head
{
this:
np:hasAssertion
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_assertion
;
np:hasProvenance
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_provenance
;
np:hasPublicationInfo
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_assertion
a
np:Assertion
.
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_provenance
a
np:Provenance
.
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_assertion
{
miriam-gene:2114
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGN2d8db8fdbfd4d4a3c7d99ea72702ac22
sio:SIO_000628
miriam-gene:2114
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_provenance
{
dgn-np:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_assertion
dcterms:description
"[These patients belong to two groups of Down syndrome patients characterized by different partial trisomies 21: (i) duplication of the long arm, proximal to 21q22.2, and (ii) duplication of the end of the chromosome, distal to 21q22.2 We assessed the copy number of five chromosome 21 sequences (SOD1, D21S17, D21S55, ETS2, and D21S15) and found that D21S55 was duplicated in both cases.]. 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:2527368
;
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:NP833232.RAm0LKXjd1mR-KzAPWrTa4R7lYbwdTneQjYAn7IipCpNM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}