@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ
> .
@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:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_head
{
this:
np:hasAssertion
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_assertion
;
np:hasProvenance
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_assertion
a
np:Assertion
.
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_provenance
a
np:Provenance
.
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_assertion
{
miriam-gene:3630
a
ncit:C16612
.
lld:C1852197
a
ncit:C7057
.
dgn-gda:DGN2d2d21b1c47084372984f8590cfc4d8f
sio:SIO_000628
miriam-gene:3630
,
lld:C1852197
;
a
sio:SIO_001121
.
}
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_provenance
{
dgn-np:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_assertion
dcterms:description
"[Reanalysis of an Old Order Amish pedigree, to include several new individuals and two changes in clinical status, markedly reduces the probability of linkage between bipolar affective disorder and the Harvey-ras-1 oncogene and insulin loci on chromosome 11.]. 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:2682265
;
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:NP912743.RABK0nEwcJqAP_N0wCDw38FqvowzTvVf7qgLJ5MRutnpQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}