Matches in Nanopublications for { ?s ?p "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 12 of
12
with 100 items per page.
- assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP396226.RAXtmL-gujCy_0f4L24MQWpGLnd9VDHGI5RIrjsDjTguo130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396226.RAXtmL-gujCy_0f4L24MQWpGLnd9VDHGI5RIrjsDjTguo130_provenance.
- NP396270.RAQj7kyskHjg6oTS7dLYrN-v0aGf9VBOC4THR8pX58gdk130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396270.RAQj7kyskHjg6oTS7dLYrN-v0aGf9VBOC4THR8pX58gdk130_provenance.
- NP1245434.RAdZQVWMsN3gjTSPuCeD1L3txEs-vnZW8Scj1H3vE6Jmc130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245434.RAdZQVWMsN3gjTSPuCeD1L3txEs-vnZW8Scj1H3vE6Jmc130_provenance.
- NP396197.RApVsrwV_ZVekovym3MinUgESTSkl1P8otPfP9OA6miUY130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396197.RApVsrwV_ZVekovym3MinUgESTSkl1P8otPfP9OA6miUY130_provenance.
- NP396204.RAOu6cCz3CmwIlum6utUSJxD9CvkwVys8bpn4go66BR4I130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP396204.RAOu6cCz3CmwIlum6utUSJxD9CvkwVys8bpn4go66BR4I130_provenance.
- NP1245435.RAPPYx8keEbRSAqGmkc4bHNSt3tUom-Kt6HjlM28xaAVg130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245435.RAPPYx8keEbRSAqGmkc4bHNSt3tUom-Kt6HjlM28xaAVg130_provenance.
- NP1245436.RAGRccCkX8_F0lbN08ZNWVgXo-7obelImw5bRN0hNwie4130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245436.RAGRccCkX8_F0lbN08ZNWVgXo-7obelImw5bRN0hNwie4130_provenance.
- NP1245433.RA4XgXiv2LWdWqlUQlJxfiIuaWiTs4p-gyMVbke30MH1M130_assertion description "[An Arg345Trp (R345W) mutation in the last canonical calcium-binding epidermal growth factor (cbEGF) domain of fibulin-3 (F3) causes the rare macular dystrophy, Malattia Leventinese (ML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245433.RA4XgXiv2LWdWqlUQlJxfiIuaWiTs4p-gyMVbke30MH1M130_provenance.