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- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion type Assertion NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_head.
- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion wasGeneratedBy ECO_0000203 NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_provenance.
- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion wasDerivedFrom befree-20150227 NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_provenance.
- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion SIO_000772 24039054 NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_provenance.
- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion evidence source_evidence_literature NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_provenance.
- NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_assertion description "[Severe congenital lipodystrophy and a progeroid appearance: Mutation in the penultimate exon of FBN1 causing a recognizable phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395899.RA4qKain344g_EO5QTPsCeizoh6E38NAMjaso_o0WMLK0130_provenance.