Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion> ?p ?o ?g. }
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- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion type Assertion NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_head.
- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion wasGeneratedBy ECO_0000203 NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_provenance.
- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion wasDerivedFrom befree-20150227 NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_provenance.
- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion SIO_000772 16459341 NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_provenance.
- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion evidence source_evidence_literature NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_provenance.
- NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_assertion description "[Mutations of human TMHS cause recessively inherited non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981012.RAaIU2p0tMCotlDYCEHxEaBW1M5x5LzWPGsaY64tqHxuw130_provenance.