Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion type Assertion NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_head.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion description "[Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion evidence source_evidence_literature NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion SIO_000772 10441342 NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion wasDerivedFrom befree-20140225 NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_assertion wasGeneratedBy ECO_0000203 NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.