@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4
> .
@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/v3.0.0/void/
> .
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_head
{
this:
np:hasAssertion
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_assertion
;
np:hasProvenance
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_provenance
;
np:hasPublicationInfo
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_assertion
a
np:Assertion
.
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_provenance
a
np:Provenance
.
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_assertion
{
miriam-gene:9499
a
ncit:C16612
.
lld:C2678065
a
ncit:C7057
.
dgn-gda:DGNb8abd649b16bc9d8031725af725cab79
sio:SIO_000628
miriam-gene:9499
,
lld:C2678065
;
a
sio:SIO_001121
.
}
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_provenance
{
dgn-np:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_assertion
dcterms:description
"[The essential role of myotilin in skeletal muscle is attested by the observation that certain forms of myofibrillar myopathy and limb girdle muscular dystrophy are caused by mutations in the human myotilin gene.]. 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:16076904
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP824764.RAPZS45n-yVR1XwBgtj8hSTp_4FDWYUH28BLaJJKfPvG4130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:00+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}