Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_assertion description "[To gain further insight into the possible role of myostatin in primary muscle diseases, the authors investigated the expression of muscle myostatin in children with congenital fiber type 1 disproportion, in others with neurogenic muscular atrophy, in others with myotonia congenita, in others with infantile glycogenosis type II, in others with Prader-Willi syndrome, and in 4 age-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_assertion evidence source_evidence_literature NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_assertion SIO_000772 17608303 NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_assertion wasDerivedFrom befree-2016 NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_assertion wasGeneratedBy ECO_0000203 NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.
- befree-2016 importedOn "2016-02-19" NP618269.RAWEsUWBk96fOheYXmycZbYR7WA_0-oGU3nZsgl6ARyXk130_provenance.