@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M
> .
@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:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_head
{
this:
np:hasAssertion
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_assertion
;
np:hasProvenance
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_provenance
;
np:hasPublicationInfo
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_assertion
a
np:Assertion
.
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_provenance
a
np:Provenance
.
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGN9a37b2dc28bbfb6bda3604cee21f82a2
sio:SIO_000628
miriam-gene:324
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_provenance
{
dgn-np:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_assertion
dcterms:description
"[We have examined 41 cases of follicle centre cell lymphoma with fluorescent PCR of microsatellite repeats closely linked to or within six tumour suppressor gene loci (APC, DCC, P53, RB1, WT1 and NM23).]. 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:8724537
;
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:NP894536.RA70BwF_8_amEAmNKwnHA3cnCna65vwvTdHOowmpADd5M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}