@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA
> .
@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:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_head
{
this:
np:hasAssertion
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion
;
np:hasProvenance
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance
;
np:hasPublicationInfo
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion
a
np:Assertion
.
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance
a
np:Provenance
.
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN36bec3514cafa7e24141ab1f1b10cb36
sio:SIO_000628
miriam-gene:4000
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_provenance
{
dgn-np:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_assertion
dcterms:description
"[These findings indicate that approximately half of the variance in mean s.c. abd. AS can be attributed to familial factors and that genetic variation in LMNA might not only underlie rare cases of FPLD, but may also contribute to variation in adipocyte size in the general population.]. 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:11243729
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP55298.RAWRR0_woIdy2228O4NTYKUF9V6we2aLjhLMINSXpXKlA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}