Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion> ?p ?o ?g. }
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- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion type Assertion NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_head.
- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion description "[We have identified previously uncharacterized NHP2 mutations that can cause autosomal recessive dyskeratosis congenita but have not found any GAR1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_provenance.
- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion evidence source_evidence_literature NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_provenance.
- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion SIO_000772 18523010 NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_provenance.
- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion wasDerivedFrom befree-20150227 NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_provenance.
- NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_assertion wasGeneratedBy ECO_0000203 NP919859.RAa3BCHLbQR4TXKNf-yY3dbXryiDPKwwZzGyoeOypm6U4130_provenance.