@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ
> .
@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:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_head
{
this:
np:hasAssertion
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_assertion
;
np:hasProvenance
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_assertion
a
np:Assertion
.
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_provenance
a
np:Provenance
.
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_assertion
{
miriam-gene:412
a
ncit:C16612
.
lld:C0795864
a
ncit:C7057
.
dgn-gda:DGN81e10fcb28cba0e71f223f5eaba57530
sio:SIO_000628
miriam-gene:412
,
lld:C0795864
;
a
sio:SIO_001121
.
}
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_provenance
{
dgn-np:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_assertion
dcterms:description
"[Moreover two YACs contain both STS deleted in SMS (U3) and STS duplicated in CMT1A (5H5), but the proximal breakpoint associated with the CMT1A duplication is not the same as the distal SMS breakpoint we studied.]. 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:8401506
;
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:NP746421.RArt9F9y8E06zTv8LJzhIeP-Z3T3kv2kz-4eJf9IiOTZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:32+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" .
}