@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94
> .
@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:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_head
{
this:
np:hasAssertion
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_assertion
;
np:hasProvenance
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_provenance
;
np:hasPublicationInfo
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_assertion
a
np:Assertion
.
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_provenance
a
np:Provenance
.
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_assertion
{
miriam-gene:55143
a
ncit:C16612
.
lld:C0265234
a
ncit:C7057
.
dgn-gda:DGN172fb4c581d4a3f0454ea29fc3630156
sio:SIO_000628
miriam-gene:55143
,
lld:C0265234
;
a
sio:SIO_001121
.
}
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_provenance
{
dgn-np:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_assertion
dcterms:description
"[This mapping led us to reevaluate the localization of the gene responsible for BOR syndrome and has now focused the search for the BOR gene to within the limits of this deletion.]. 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:8786145
;
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:NP167613.RADz2-YN7C9zIEuR0vEFQTGUoON-IQrWW6_P6bwuXVs94130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}