@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs
> .
@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:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_head
{
this:
np:hasAssertion
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_assertion
;
np:hasProvenance
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_provenance
;
np:hasPublicationInfo
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_assertion
a
np:Assertion
.
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_provenance
a
np:Provenance
.
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_assertion
{
miriam-gene:585
a
ncit:C16612
.
lld:C0752166
a
ncit:C7057
.
dgn-gda:DGN46d22e657f7af1da3da7f624c4397faf
sio:SIO_000628
miriam-gene:585
,
lld:C0752166
;
a
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.
}
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_provenance
{
dgn-np:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_assertion
dcterms:description
"[Here we report that despite tissue specific variable expression of the transgene, human BBS4 was able to complement the deficiency of Bbs4 and rescue all the BBS phenotypes in the Bbs4 null mice.]. 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:23554981
;
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:NP294289.RA9MK868Jk2OJk1m8aXQ4YbKkq28ACI7bRnJXKPA3-Lgs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}