Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP881803.RAWN2RoV_QsnNuc90mHTRHCxYQvvUvQ2H8KNPT8UeWB4o130_provenance.