@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA
> .
@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:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_head
{
this:
np:hasAssertion
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_assertion
;
np:hasProvenance
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_provenance
;
np:hasPublicationInfo
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_assertion
a
np:Assertion
.
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_provenance
a
np:Provenance
.
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_assertion
{
miriam-gene:4312
a
ncit:C16612
.
lld:C0086525
a
ncit:C7057
.
dgn-gda:DGN152a31312c4a52d6111e5d5942e9c0ec
sio:SIO_000628
miriam-gene:4312
,
lld:C0086525
;
a
sio:SIO_001121
.
}
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_provenance
{
dgn-np:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_assertion
dcterms:description
"[Moreover, there was a dramatic increase in the gene expression and activity of matrix metalloproteinase 1, which may contribute to the cytoskeleton remodeling involved in the weakness and atrophy of muscle commonly seen in MERRF patients.]. 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:20411357
;
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:NP834958.RAtj6pVi3IV8Nm9F6D0Wq-W5Nw1h2-H1kj7Gznm99hOkA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:31+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" .
}