Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_assertion description "[Mutations in myotilin gene (MYOT) have been associated with variable syndromes including limb girdle muscular dystrophy type 1A (LGMD1A) and a subgroup of myofibrillar myopathy (MFM/MYOT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_assertion evidence source_evidence_literature NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_assertion SIO_000772 15947064 NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_assertion wasDerivedFrom befree-2016 NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_assertion wasGeneratedBy ECO_0000203 NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.
- befree-2016 importedOn "2016-02-19" NP498683.RARxAb7UzATCeomV1JG8fl4Trej0B5w1qooeIjx9J6-2w130_provenance.