Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion> ?p ?o ?g. }
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- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion type Assertion NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_head.
- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion wasGeneratedBy ECO_0000203 NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_provenance.
- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion wasDerivedFrom befree-20150227 NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_provenance.
- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion SIO_000772 12868035 NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_provenance.
- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion evidence source_evidence_literature NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_provenance.
- NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_assertion description "[We screened the OA1 gene for mutations in three unrelated Canadian and French families and in two isolated patients with OA1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002290.RA4kkRB_5AGgwCWALCGLax4h7QdDLqfRT7JisKHhP-KFY130_provenance.