Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion> ?p ?o ?g. }
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- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion type Assertion NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_head.
- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_provenance.
- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion evidence source_evidence_literature NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_provenance.
- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion SIO_000772 23304067 NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_provenance.
- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion wasDerivedFrom befree-20150227 NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_provenance.
- NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_assertion wasGeneratedBy ECO_0000203 NP767634.RAY56y-I_NfFO78xMfGegA4D9IDRmhrZy7wWd4VQU3394130_provenance.