@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc
> .
@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:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_head
{
this:
np:hasAssertion
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion
;
np:hasProvenance
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance
;
np:hasPublicationInfo
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion
a
np:Assertion
.
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance
a
np:Provenance
.
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion
{
miriam-gene:4843
a
ncit:C16612
.
lld:C0020981
a
ncit:C7057
.
dgn-gda:DGNcaf97e8b077cf93ea4c7743e6477edc9
sio:SIO_000628
miriam-gene:4843
,
lld:C0020981
;
a
sio:SIO_001121
.
}
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_provenance
{
dgn-np:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_assertion
dcterms:description
"[The recent identification of follicular helper T (T(FH)) cell as the cell of origin of this neoplasm represents a major step in our understanding of the pathobiological characteristics of the disease and should, in the future, clarify the diagnostic criteria for AITL and help to delineate its spectrum, especially from PTCL, not otherwise specified (PTCL, NOS).]. 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:19961485
;
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:NP508839.RADkrMergAVTBkVvTG8aBMzWPf3Ipe8FoVKCgSzGrEzGc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}