Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion type Assertion NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_head.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion description "[A 263 Kb homozygous deletion of FMN1 was associated with oligosyndactyly, radioulnar synostosis, hearing loss and renal defects, features identical to ld mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion evidence source_evidence_literature NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion SIO_000772 20610440 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion wasDerivedFrom befree-20140225 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.
- NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_assertion wasGeneratedBy ECO_0000203 NP583435.RAX5Gly88hGEgzSkw5Q7j-7Cs04Zk_GiiLzACaOKZ6iio130_provenance.