Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion> ?p ?o ?g. }
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- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion type Assertion NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_head.
- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion wasGeneratedBy ECO_0000203 NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_provenance.
- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion wasDerivedFrom befree-20140225 NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_provenance.
- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion SIO_000772 11968094 NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_provenance.
- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion evidence source_evidence_literature NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_provenance.
- NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_assertion description "[A HOXA13 allele with a missense mutation in the homeobox and a dinucleotide deletion in the promoter underlies Guttmacher syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP398685.RAjYbffLwEa5vgRyMWFXugeLOHeO21LCnBz8c8F7AWY0g130_provenance.