@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0
> .
@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:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_head
{
this:
np:hasAssertion
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_assertion
;
np:hasProvenance
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_provenance
;
np:hasPublicationInfo
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_assertion
a
np:Assertion
.
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_provenance
a
np:Provenance
.
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_assertion
{
miriam-gene:23512
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNcbdbb982761e7a830c85b16175f15299
sio:SIO_000628
miriam-gene:23512
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_provenance
{
dgn-np:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_assertion
dcterms:description
"[Here we show that SUZ12 is anomalously expressed in human primary tumors, especially in mantle cell lymphoma (MCL), pulmonary carcinomas and melanoma, and is associated with gene locus amplification in some cases.]. 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:20558579
;
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:NP729532.RAlFe1KoLHGYJ5HvcyPTGeeygbH4z05Lnzc2rEjPcJ6-0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}