Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion type Assertion NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_head.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion description "[This finding makes the ARX dup24 mutation the most common mutation in nonsyndromic XLMR families linked to Xp22.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_provenance.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion evidence source_evidence_literature NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_provenance.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion SIO_000772 15850492 NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_provenance.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion wasDerivedFrom befree-2016 NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_provenance.
- NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_assertion wasGeneratedBy ECO_0000203 NP491352.RA3Sr8DnWMY4GUNUilVBxNk4qfNZSb8Ku8NggMuW4n_r4130_provenance.