@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8
> .
@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:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_head
{
this:
np:hasAssertion
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_assertion
;
np:hasProvenance
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_provenance
;
np:hasPublicationInfo
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_assertion
a
np:Assertion
.
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_provenance
a
np:Provenance
.
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0007120
a
ncit:C7057
.
dgn-gda:DGN5f151ecdb1e7b0c1026b0cbec4bf1ccb
sio:SIO_000628
miriam-gene:595
,
lld:C0007120
;
a
sio:SIO_001121
.
}
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_provenance
{
dgn-np:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_assertion
dcterms:description
"[Fluorescence in situ hybridization using bacterial artificial chromosome (BAC) clones showed that the 11q13 breakpoints in all three tumors were near the CCND1 (previously BCL1) gene and did not disrupt any other known gene.]. 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:15036887
;
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:NP189088.RA9Gp2RyKSEd4wjuRch72fmtz4OFLl8rq1qMwsvyJCu-8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}