@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0
> .
@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:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_head
{
this:
np:hasAssertion
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_assertion
;
np:hasProvenance
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_assertion
a
np:Assertion
.
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_provenance
a
np:Provenance
.
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_assertion
{
miriam-gene:10554
a
ncit:C16612
.
lld:C0023787
a
ncit:C7057
.
dgn-gda:DGNcd92a5affdb4e18229ada832066aba8c
sio:SIO_000628
miriam-gene:10554
,
lld:C0023787
;
a
sio:SIO_001121
.
}
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_provenance
{
dgn-np:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_assertion
dcterms:description
"[In this study, we have performed mutation screening in AGPAT2 and the related AGPAT1 in patients with BSCL or other forms of lipodystrophy who have no detectable mutation in the seipin gene.]. 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:12765973
;
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:NP284847.RA5YxS-qDF0Wh7cn7WPWszxLUZcrL8wZLG_KVR9m55Sv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}