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- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion type Assertion NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_head.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion description "[C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion evidence source_evidence_literature NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion SIO_000772 25729264 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion wasDerivedFrom befree-2016 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.
- NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_assertion wasGeneratedBy ECO_0000203 NP1267337.RAEL8_nX2ldrr8BZR5SZbjbQ5N4XEBgLeq-hMUTsTGpAc130_provenance.