@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY
> .
@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:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_head
{
this:
np:hasAssertion
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_assertion
;
np:hasProvenance
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_provenance
;
np:hasPublicationInfo
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_assertion
a
np:Assertion
.
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_provenance
a
np:Provenance
.
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN474670847f006915a6ba0fe5addb656f
sio:SIO_000628
miriam-gene:6520
,
lld:C0026848
;
a
sio:SIO_001121
.
}
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_provenance
{
dgn-np:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_assertion
dcterms:description
"[Our results provide evidence that the pathogenesis of the MyHC IIa E706K myopathy involves defective function of the mutated myosin as well as alterations in the structural integrity of all muscle cells irrespective of MyHC isoform expression.]. 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:17005402
;
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:NP547292.RAri2do37FRf2x4iQku1JyLfrvmnWx3xmV94F75l6-wMY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
}