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- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion type Assertion NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_head.
- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion description "[Missense mutations of ACTA1 cause dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_provenance.
- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion evidence source_evidence_curated NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_provenance.
- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion SIO_000772 15520409 NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_provenance.
- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion wasDerivedFrom uniprot-2016 NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_provenance.
- NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_assertion wasGeneratedBy ECO_0000218 NP3727.RAxf7g37Smpj5OcS_YSPlvl4DjnWFdctALJQJ3-M05HT4130_provenance.