Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_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." NP663689.RACW82R_zxPNLTunCcu82VzH1-Lr9hY6sVuStNA7HLAcA130_provenance.
- 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." provenance.
- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_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." NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_provenance.
- NP1208198.RATT-reIDYsyO3xGxi5MW8YXNLDYYpRz2jxFl_SPprFgM130_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." NP1208198.RATT-reIDYsyO3xGxi5MW8YXNLDYYpRz2jxFl_SPprFgM130_provenance.
- 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." provenance.
- 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.