Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion> ?p ?o ?g. }
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- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion type Assertion NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_head.
- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion description "[Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_provenance.
- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion evidence source_evidence_literature NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_provenance.
- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion SIO_000772 23222558 NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_provenance.
- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion wasDerivedFrom befree-2016 NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_provenance.
- NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_assertion wasGeneratedBy ECO_0000203 NP1034381.RAkn2cIH2K89dfnUOATXqx2BNI_BZSUw4RC7jOSnJc1OQ130_provenance.