Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion> ?p ?o ?g. }
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- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion type Assertion NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_head.
- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion wasGeneratedBy ECO_0000203 NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_provenance.
- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion wasDerivedFrom befree-2016 NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_provenance.
- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion SIO_000772 19860667 NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_provenance.
- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion evidence source_evidence_literature NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_provenance.
- NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_assertion description "[Non-syndromic, hereditary human cataract development is linked to point mutations in the CRYAA and CRYAB genes which encode alphaA and alphaB-crystallin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771962.RAcdT7YaJGi3grswhGFNETJIzwfO_ws5fjKULMUcxVb94130_provenance.