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- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion type Assertion NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_head.
- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion description "[By WES and filtering with a mining tool, a novel FBN1 missense variant was found in patient 1 and his mother, who both showed clinical features of Marfan syndrome by thorough anthropometric assessment, and a novel EYA1 missense variant as a probable cause of the renal malformation in the patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_provenance.
- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion evidence source_evidence_literature NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_provenance.
- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion SIO_000772 23552953 NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_provenance.
- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion wasDerivedFrom befree-2016 NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_provenance.
- NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_assertion wasGeneratedBy ECO_0000203 NP1066046.RAO1NCENuPSq_rLY3xF_jx2_lx1sDQwhDH3Ao8rkTCSYY130_provenance.