Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion> ?p ?o ?g. }
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- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion type Assertion NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_head.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion description "[These findings question p.I148T or p.R74W-p.D1270N as causing by themselves CF or CBAVD and emphazises the necessity to perform a complete scanning of CFTR genes and to assign the parental alleles when novel missense mutations are identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion evidence source_evidence_literature NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion SIO_000772 15287992 NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion wasDerivedFrom befree-20140225 NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.
- NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_assertion wasGeneratedBy ECO_0000203 NP184461.RASYcK7QiNuPq3d4cWvwbPn4yJgiU96WWbm3m6LMhbz0k130_provenance.