Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion> ?p ?o ?g. }
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- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion type Assertion NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_head.
- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion wasGeneratedBy ECO_0000203 NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_provenance.
- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion wasDerivedFrom befree-20150227 NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_provenance.
- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion SIO_000772 25098561 NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_provenance.
- NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_assertion evidence source_evidence_literature NP348129.RANEBwIx97U4KSlZc5dBmkU-Tu0OWnsssaBx7XYQ5bkFM130_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.