Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion> ?p ?o ?g. }
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- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion type Assertion NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_head.
- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion description "[Mutations in human AHI1 underlie the autosomal recessive Joubert Syndrome with brain malformation and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_provenance.
- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion evidence source_evidence_literature NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_provenance.
- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion SIO_000772 16773125 NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_provenance.
- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion wasDerivedFrom befree-20140225 NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_provenance.
- NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_assertion wasGeneratedBy ECO_0000203 NP885489.RAlUqlv63OzmUILccSFTrhWOtMFlnjPnm7xbO-FjcxdKE130_provenance.