@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78
> .
@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:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_head
{
this:
np:hasAssertion
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_assertion
;
np:hasProvenance
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_provenance
;
np:hasPublicationInfo
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_assertion
a
np:Assertion
.
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_provenance
a
np:Provenance
.
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_assertion
{
miriam-gene:4312
a
ncit:C16612
.
lld:C0162672
a
ncit:C7057
.
dgn-gda:DGNca446663e23b9d3c49117532ff6c3d4a
sio:SIO_000628
miriam-gene:4312
,
lld:C0162672
;
a
sio:SIO_001121
.
}
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_provenance
{
dgn-np:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_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:NP813966.RAn9B_OgAE_X9yKAVOgqEy_ocdyLt3COCsL_1OKGs3w78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}