Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_assertion description "[The allelic muscle disorders known as limb-girdle muscular dystrophy type 2B (LGMD2B), Miyoshi myopathy and distal anterior compartment myopathy result from defects in dysferlin-a sarcolemma-associated protein involved in membrane repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_assertion evidence source_evidence_literature NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_assertion SIO_000772 20535123 NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_assertion wasDerivedFrom befree-2016 NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_assertion wasGeneratedBy ECO_0000203 NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP817614.RAf3lEg_s3tIdRX71W3XpM13go6VLKCPmvsAfGySoFO4Q130_provenance.