@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98
> .
@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:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_head
{
this:
np:hasAssertion
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion
;
np:hasProvenance
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance
;
np:hasPublicationInfo
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion
a
np:Assertion
.
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance
a
np:Provenance
.
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion
{
miriam-gene:7389
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGNfed599aee78ce941dbe4d28eab091acf
sio:SIO_000628
miriam-gene:7389
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_provenance
{
dgn-np:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_assertion
dcterms:description
"[PCR amplification of polymorphic loci mapping to 11p15.5 region documented partial trisomy of 11p15.5 due to paternal translocation in one, and segmental and mosaic segmental unipaternal disomy (UPD) in the second and third cases, respectively.]. 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:11807901
;
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:NP532539.RA-4_GYIQ87l8A3tFilIBXM1P6q0fGcgIGLXY5XZl0m98130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}