Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion> ?p ?o ?g. }
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- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion type Assertion NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_head.
- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion wasGeneratedBy ECO_0000218 NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_provenance.
- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion wasDerivedFrom ctd_human-20130708 NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_provenance.
- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion SIO_000772 21725307 NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_provenance.
- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion evidence source_evidence_curated NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_provenance.
- NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_assertion description "[Consistent with a shared function for complex components, we identified a mutation in TCTN1 that causes Joubert syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP31447.RAeC7EC7CO--r6QNH6ttAvkiljtd-mvXKpzK4eZFr9Qsw130_provenance.