@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c
> .
@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:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_head
{
this:
np:hasAssertion
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_assertion
;
np:hasProvenance
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_assertion
a
np:Assertion
.
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_provenance
a
np:Provenance
.
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_assertion
{
miriam-gene:7203
a
ncit:C16612
.
lld:C2931689
a
ncit:C7057
.
dgn-gda:DGN21ad3b0092b4b94c0787edf2febb413e
sio:SIO_000628
miriam-gene:7203
,
lld:C2931689
;
a
sio:SIO_001121
.
}
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_provenance
{
dgn-np:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_assertion
dcterms:description
"[Electrophoresis and visualisation of PCR products on an automatic sequencer were applied to determine normal and pathogenic alleles comprising (C4GC4GCG)n in EPM1 in 44 subjects, (CCTG)n in DM2 in 76 individuals and (CTG)n in SCA8 in 378 patients.]. 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:22581592
;
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:NP403601.RAAdUmBQqjKLCEjL8k7atgSSEp_djiuqMY0GOPHcCKn4c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}