@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE
> .
@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:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_head
{
this:
np:hasAssertion
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_assertion
;
np:hasProvenance
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_provenance
;
np:hasPublicationInfo
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_assertion
a
np:Assertion
.
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_provenance
a
np:Provenance
.
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0026948
a
ncit:C7057
.
dgn-gda:DGNd8897c5755c22553ce5394c08e170cc9
sio:SIO_000628
miriam-gene:920
,
lld:C0026948
;
a
sio:SIO_001121
.
}
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_provenance
{
dgn-np:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_assertion
dcterms:description
"[Nine of 17 cases showed the characteristic clinical and histological features as well as clinical behavior of well defined types of CTCL, such as mycosis fungoides (2 cases), pagetoid reticulosis (2 cases), lymphomatoid papulosis (2 cases), and CD30+ large T cell lymphoma (2 cases), all of which usually express a CD4+ T cell phenotype, and 1 case of subcutaneous panniculitis-like T cell lymphoma.]. 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:10433941
;
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:NP605384.RAUac9X2Zv1dt5lfh6OICC7UTQbrRc_3CaRDfRBB0ZycE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}