Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion> ?p ?o ?g. }
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- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion type Assertion NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_head.
- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion description "[Mutations in the human RDS gene are responsible for several forms of inherited blindness including autosomal-dominant retinitis pigmentosa and macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_provenance.
- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion evidence source_evidence_literature NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_provenance.
- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion SIO_000772 10704489 NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_provenance.
- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion wasDerivedFrom befree-20140225 NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_provenance.
- NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_assertion wasGeneratedBy ECO_0000203 NP692768.RAPJOBaSC9eYV_NqFygyyim4lz38uQR61ELagP0pVIloI130_provenance.