Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion type Assertion NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_head.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion description "[By sequencing candidate genes, we identified recessive LRP4 mutations in 12 families with CLS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion evidence source_evidence_literature NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion SIO_000772 20381006 NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion wasDerivedFrom befree-20140225 NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_assertion wasGeneratedBy ECO_0000203 NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.