@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE
> .
@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:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_head
{
this:
np:hasAssertion
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_assertion
;
np:hasProvenance
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_provenance
;
np:hasPublicationInfo
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_assertion
a
np:Assertion
.
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_provenance
a
np:Provenance
.
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_assertion
{
miriam-gene:1637
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGN855dda7910b3f2946a7d84fab4b38789
sio:SIO_000628
miriam-gene:1637
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_provenance
{
dgn-np:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_assertion
dcterms:description
"[The translocation breakpoint of 21q for each patient was located on the centromeric side of DSCR (DSCR was deleted) and the sizes of partial trisomy 21 in respective patients are approximately 34.5 (21pter-q22.12) and approximately 33.0 Mb (21pter-q22.11).]. 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:16411203
;
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:NP442655.RA-m12IgJZvt4CzvnTQu4WikgS9nfxlk44gaixTI6LxIE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:24+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" .
}