Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP308939.RAefsBpyhxUoa1m_aKMa8QKSXGELauv4GBRK5Q32AguQo130_provenance.