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- source_evidence_literature type ECO_0000212 NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion description "[A complex phenotype of peripheral neuropathy, myopathy, hoarseness, and hearing loss is linked to an autosomal dominant mutation in MYH14.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion evidence source_evidence_literature NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion SIO_000772 21480433 NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion wasDerivedFrom befree-20150227 NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_assertion wasGeneratedBy ECO_0000203 NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP945574.RATNxE6zpN6hz-9GPof9PL8X6VLpQz9P3jgyju25ar7OU130_provenance.