Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion> ?p ?o ?g. }
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- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion type Assertion NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_head.
- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion description "[LAP2 mutations may represent a rare cause of DCM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_provenance.
- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion evidence source_evidence_literature NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_provenance.
- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion SIO_000772 16247757 NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_provenance.
- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion wasDerivedFrom befree-2016 NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_provenance.
- NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_assertion wasGeneratedBy ECO_0000203 NP519510.RAMhAI2b8QTUAk2tRH3oQKkMNkRtJyhjQdpPW_Yzjn_a8130_provenance.