@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY
> .
@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:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_head
{
this:
np:hasAssertion
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_assertion
;
np:hasProvenance
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_provenance
;
np:hasPublicationInfo
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_assertion
a
np:Assertion
.
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_provenance
a
np:Provenance
.
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0340427
a
ncit:C7057
.
dgn-gda:DGNe78863d4b094bb91d0cbda6ce248777d
sio:SIO_000628
miriam-gene:4000
,
lld:C0340427
;
a
sio:SIO_001121
.
}
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_provenance
{
dgn-np:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_assertion
dcterms:description
"[It is still not at all clear how defects in these nuclear membrane proteins are related to the phenotype, even less clear that LMNA mutations can also be associated with familial dilated cardiomyopathy with no weakness, and even familial partial lipodystrophy with diabetes mellitus and coronary heart disease!]. 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:10838246
;
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:NP516340.RACtln7xGk44cHX6dO4cI1Ju5Cu8sYi6Bm1oNtF1M4UTY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:07+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" .
}