Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion> ?p ?o ?g. }
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- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion type Assertion NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_head.
- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion description "[Using a linkage analysis and a candidate gene approach, two genes have been implicated in congenital MRMV disorder to date: DCC on 18q21.2 (MRMV1), which encodes a netrin receptor, and RAD51 on 15q15.1 (MRMV2), which is involved in the maintenance of genomic integrity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_provenance.
- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion evidence source_evidence_literature NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_provenance.
- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion SIO_000772 25098561 NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_provenance.
- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion wasDerivedFrom befree-2016 NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_provenance.
- NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_assertion wasGeneratedBy ECO_0000203 NP1208199.RALLfmQOlnYjvw1fat4095hGBzyl-AAMBMS55m-hWthmg130_provenance.