@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM
> .
@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:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_head
{
this:
np:hasAssertion
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_assertion
;
np:hasProvenance
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_provenance
;
np:hasPublicationInfo
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_assertion
a
np:Assertion
.
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_provenance
a
np:Provenance
.
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_assertion
{
miriam-gene:1649
a
ncit:C16612
.
lld:C0206651
a
ncit:C7057
.
dgn-gda:DGNeb0ae7e5c342153c13ae3d68b1411f9f
sio:SIO_000628
miriam-gene:1649
,
lld:C0206651
;
a
sio:SIO_001121
.
}
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_provenance
{
dgn-np:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_assertion
dcterms:description
"[Restriction fragment analysis showed that the CHOP gene and its flanking sequences were not rearranged in any of these tumor types, indicating that the 12q translocation breakpoints in pleomorphic adenoma and clear-cell sarcoma are different from that in myxoid liposarcoma.]. 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:7687873
;
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:NP557822.RAkMvth5Mw26A8yr4U-n_fCJ-JeljgLjaBfnxUbYaEamM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}