@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ
> .
@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:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_head
{
this:
np:hasAssertion
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion
;
np:hasProvenance
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion
a
np:Assertion
.
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance
a
np:Provenance
.
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion
{
miriam-gene:923
a
ncit:C16612
.
lld:C0280100
a
ncit:C7057
.
dgn-gda:DGN2d7c9d95951f6e9522d93329bda2ac8b
sio:SIO_000628
miriam-gene:923
,
lld:C0280100
;
a
sio:SIO_001121
.
}
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_provenance
{
dgn-np:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_assertion
dcterms:description
"[Furthermore, FISH analysis using cosmid LLNL12-NCO1-144G3, which maps at the CHOP locus, revealed that the chromosome 12 breakpoints in all cell lines of the three benign solid tumors that were tested were located distal to the chromosome 12 translocation breakpoint with the CHOP gene in myxoid liposarcoma cells with t(12;16).]. 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:8020967
;
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:NP790040.RAxz8Y8GAZvHDNf1a1wXbSAKqdwrL4wyKkhwTG9eq7UgQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}