@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI
> .
@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:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_head
{
this:
np:hasAssertion
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_assertion
;
np:hasProvenance
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_assertion
a
np:Assertion
.
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_provenance
a
np:Provenance
.
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_assertion
{
miriam-gene:118460
a
ncit:C16612
.
lld:C0039101
a
ncit:C7057
.
dgn-gda:DGN08ef1f86111f422d0c92c53414879ef4
sio:SIO_000628
miriam-gene:118460
,
lld:C0039101
;
a
sio:SIO_001121
.
}
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_provenance
{
dgn-np:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_assertion
dcterms:description
"[The t(X;18)(p11.2;q11.2) translocation commonly found in synovial sarcoma (SS) results in the fusion of the SYT gene on chromosome 18 to either of two closely related genes, SSX1 and SSX2, on chromosome X.]. 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:10824918
;
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:NP256338.RAXW_LxPhrWqltGxbtmhG9I68j5Znk7O9TGod3AUw1fNI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}