@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8
> .
@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:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_head
{
this:
np:hasAssertion
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_assertion
;
np:hasProvenance
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_provenance
;
np:hasPublicationInfo
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_assertion
a
np:Assertion
.
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_provenance
a
np:Provenance
.
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNc1234825668f66bb50cd058424311811
sio:SIO_000628
miriam-gene:3133
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_provenance
{
dgn-np:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_assertion
dcterms:description
"[Twenty-four cases of histologically defined follicle centre cell (FCC) lymphoma have been examined for allele imbalance at 19 microsatellite loci spanning the length of chromosome 6, including six markers within the major histocompatibility complex (MHC), using fluorescent polymerase chain reaction (PCR) to amplify microsatellites.]. 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:8826862
;
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:NP351417.RA388_EJlQliKxAkdNUBhdkKwxdEvZLzeMmGli4DV8WB8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}