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- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion type Assertion NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_head.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion wasGeneratedBy ECO_0000203 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion wasDerivedFrom befree-20140225 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion SIO_000772 16533976 NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion evidence source_evidence_literature NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.
- NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_assertion description "[Classic Fabry disease, an X-linked recessive lysosomal storage disease due to the deficient activity of alpha-galactosidase A, typically presents in early childhood with acroparesthesias, angiokeratomas, hypohidrosis, and corneal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817695.RAWEP8f2Rvnvwwvzkyz9LkNfHUsnNKdZl0UrvbT_ZZ_pk130_provenance.