@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg
> .
@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:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_head
{
this:
np:hasAssertion
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion
;
np:hasProvenance
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance
;
np:hasPublicationInfo
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion
a
np:Assertion
.
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance
a
np:Provenance
.
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0151786
a
ncit:C7057
.
dgn-gda:DGN74f01a4c3fa8cca53e417436bfba833e
sio:SIO_000628
miriam-gene:5972
,
lld:C0151786
;
a
sio:SIO_001121
.
}
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_provenance
{
dgn-np:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_assertion
dcterms:description
"[These findings suggest a novel mechanism, involving the renin-angiotensin system, in the response of skeletal muscle to functional overload and may have implications for the management of conditions such as muscle wasting disorders, prolonged bed rest, ageing and rehabilitation, where muscle weakness may limit function.]. 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:11038409
;
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:NP499800.RAZJJc8nQamHvI-tPES9K_2-O7qIdI26Mw0lbfskFMcPg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}