@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA
> .
@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:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_head
{
this:
np:hasAssertion
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_assertion
;
np:hasProvenance
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_assertion
a
np:Assertion
.
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_provenance
a
np:Provenance
.
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_assertion
{
miriam-gene:58
a
ncit:C16612
.
lld:C0151786
a
ncit:C7057
.
dgn-gda:DGN8f27a2680c16305a2a89905e1e67270a
sio:SIO_000628
miriam-gene:58
,
lld:C0151786
;
a
sio:SIO_001121
.
}
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_provenance
{
dgn-np:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_assertion
dcterms:description
"[Despite extensive research into normal actin function and the functional consequences of ACTA1 mutations in cell culture, animal models and patient tissue, the mechanisms underlying muscle weakness and the formation of structural lesions remains largely unknown.]. 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:22825594
;
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:NP481644.RAWgWt6cQU407IHtaHIbZh64Uucazx-pWGg6mOr4gUPNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}