@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4
> .
@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:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_head
{
this:
np:hasAssertion
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_assertion
;
np:hasProvenance
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_assertion
a
np:Assertion
.
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_provenance
a
np:Provenance
.
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_assertion
{
miriam-gene:2010
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGN069defad97ec2d1b45be6b8aa67f0c52
sio:SIO_000628
miriam-gene:2010
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_provenance
{
dgn-np:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_assertion
dcterms:description
"[This suggests that emerin is not necessary for localizing chromosomes at the nuclear periphery and that the muscular dystrophy phenotype in such individuals is not due to grossly altered nuclear organization of chromatin.]. 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:11159939
;
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:NP644577.RAQ6L7FJcg-KcOSh1vHHgzxv31XtfQlS-tGsHlh3_HzT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}