Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion> ?p ?o ?g. }
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- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion type Assertion NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_head.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion description "[Phenotypic variability in patients with retinal dystrophies due to mutations in CRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion evidence source_evidence_literature NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion SIO_000772 20956273 NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion wasDerivedFrom befree-20150227 NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.
- NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_assertion wasGeneratedBy ECO_0000203 NP872588.RAiAiK1N2QXLFX7QhFf3FlZJNHKZpHeFP241ch8vHqhK4130_provenance.