@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I
> .
@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:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_head
{
this:
np:hasAssertion
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_assertion
;
np:hasProvenance
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_provenance
;
np:hasPublicationInfo
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_assertion
a
np:Assertion
.
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_provenance
a
np:Provenance
.
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_assertion
{
miriam-gene:80896
a
ncit:C16612
.
lld:C1970945
a
ncit:C7057
.
dgn-gda:DGN99a353f9981f43ca3b0a760a6df025f9
sio:SIO_000628
miriam-gene:80896
,
lld:C1970945
;
a
sio:SIO_001121
.
}
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_provenance
{
dgn-np:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_assertion
dcterms:description
"[Although the heterogeneity analysis produced less impressive results (highest NPL score of 3.32) and a less consistent picture, we achieved evidence of locus heterogeneity at chromosomes 2q, 6p, 11p, 13q, and 22q, which was supported by adjacent markers within each region and by previously reported BPAD linkage findings.]. 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:17924339
;
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:NP247278.RA7w3bzTg7zG6pFW-daIUjr9m49a9JAccq0cXg7hmOk1I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}