@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY
> .
@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:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_head
{
this:
np:hasAssertion
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_assertion
;
np:hasProvenance
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_provenance
;
np:hasPublicationInfo
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_assertion
a
np:Assertion
.
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_provenance
a
np:Provenance
.
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_assertion
{
miriam-gene:2242
a
ncit:C16612
.
lld:C0005859
a
ncit:C7057
.
dgn-gda:DGN6de6c492aa3b5dbe708852a53d09cd2c
sio:SIO_000628
miriam-gene:2242
,
lld:C0005859
;
a
sio:SIO_001121
.
}
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_provenance
{
dgn-np:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_assertion
dcterms:description
"[Linkage disequilibrium between BLM and FES was detected in Ashkenazi Jews with BS, confirming the linkage results and supporting the hypothesis that the increased frequency of the BS mutation in the Ashkenazim is due to founder effect.]. 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:8875252
;
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:NP685658.RAgAh0cJznlBQZfvAHJdOk6zaspLR5cJ4I3N1xe9a89yY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}