Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion> ?p ?o ?g. }
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- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion type Assertion NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_head.
- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion description "[A novel missense SNRNP200 mutation associated with autosomal dominant retinitis pigmentosa in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_provenance.
- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion evidence source_evidence_curated NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_provenance.
- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion SIO_000772 23029027 NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_provenance.
- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion wasDerivedFrom uniprot-2016 NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_provenance.
- NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_assertion wasGeneratedBy ECO_0000218 NP7235.RAaGmWIHfiKn5qE2RgtC_Hf6XhhoRj7ZmJOMlgVwh6Tpo130_provenance.