Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion> ?p ?o ?g. }
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- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion type Assertion NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_head.
- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion wasGeneratedBy ECO_0000203 NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_provenance.
- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion wasDerivedFrom befree-20150227 NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_provenance.
- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion SIO_000772 11548735 NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_provenance.
- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion evidence source_evidence_literature NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_provenance.
- NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_assertion description "[These eight NCL forms resulted from 100 different mutations on genes CLN1to CLN8 causing different phenotypes (http://www.ucl.ac.uk/ncl).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP377687.RATPis6oOaiWlHcdh4igZio3Fdp9LIG6Ac-wmTLZlNEV0130_provenance.