@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo
> .
@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:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_head
{
this:
np:hasAssertion
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_assertion
;
np:hasProvenance
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_provenance
;
np:hasPublicationInfo
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_assertion
a
np:Assertion
.
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_provenance
a
np:Provenance
.
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_assertion
{
miriam-gene:5339
a
ncit:C16612
.
lld:C2931072
a
ncit:C7057
.
dgn-gda:DGNc0ec187ae5e522bd72da3b76a528ec49
sio:SIO_000628
miriam-gene:5339
,
lld:C2931072
;
a
sio:SIO_001121
.
}
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_provenance
{
dgn-np:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_assertion
dcterms:description
"[Thus plectin immunofluorescence, combined with identification of the underlying plectin mutations, is of value in predicting the severity of the muscle involvement that occurs later in life of patients with EBS-MD.]. 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:10570379
;
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:NP572456.RAk8Udz7nYgGJV6E-LhsH32dGaAv7nD7yAMhSDiZ8_CNo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:45+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" .
}