@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_head
{
this:
np:hasAssertion
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_assertion
;
np:hasProvenance
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_provenance
;
np:hasPublicationInfo
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_assertion
a
np:Assertion
.
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_provenance
a
np:Provenance
.
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_assertion
{
miriam-gene:4620
a
ncit:C16612
.
lld:C0026848
a
ncit:C7057
.
dgn-gda:DGN173937c20aeb03dbaeef969a3d016ac3
sio:SIO_000628
miriam-gene:4620
,
lld:C0026848
;
a
sio:SIO_001122
.
}
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_provenance
{
dgn-np:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP571572.RAUiNIVashAcOPNcuwhueUfCmU6lmUd5S4dvrdtcXvTW0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:04+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}