Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion> ?p ?o ?g. }
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- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion type Assertion NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_head.
- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion description "[Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_provenance.
- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion evidence source_evidence_curated NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_provenance.
- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion SIO_000772 24140113 NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_provenance.
- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion wasDerivedFrom uniprot-20150221 NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_provenance.
- NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_assertion wasGeneratedBy ECO_0000218 NP4988.RAKSbxp5fNutYfqAtohgb9Oe7Upaz7uns1p0-jEAfP9SQ130_provenance.