Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion> ?p ?o ?g. }
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- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion type Assertion NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_head.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion description "[Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion evidence source_evidence_curated NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion SIO_000772 16453125 NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion wasDerivedFrom uniprot-20150221 NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.
- NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_assertion wasGeneratedBy ECO_0000218 NP862.RAinmVBmeTm7Xrd9d1fNte80n6vtyixfoDlJncU07dhQE130_provenance.