Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion> ?p ?o ?g. }
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- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion type Assertion NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_head.
- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion description "[Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_provenance.
- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion evidence source_evidence_literature NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_provenance.
- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion SIO_000772 19508969 NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_provenance.
- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion wasDerivedFrom befree-2016 NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_provenance.
- NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_assertion wasGeneratedBy ECO_0000203 NP744119.RAtOp4LsNK9BXShc3Z4YYe2yta3-DuMXP1L_dAlv2IzeI130_provenance.