Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion description "[FHL1 mutations cause Emery-Dreifuss muscular dystrophy (OMIM 310300), X-linked myopathy with postural muscle atrophy (XMPMA, OMIM 300696), scapuloperoneal myopathy (OMIM 300695), or reducing body myopathy (OMIM 300717, 300718).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion evidence source_evidence_literature NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion SIO_000772 21932316 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion wasDerivedFrom befree-20150227 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_assertion wasGeneratedBy ECO_0000203 NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446461.RA9smcv6UVcQa2ScJS2PlWl4miVpwtaVIykppUUOnVMaI130_provenance.