Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion> ?p ?o ?g. }
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- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion type Assertion NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_head.
- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion wasGeneratedBy ECO_0000203 NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_provenance.
- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion wasDerivedFrom befree-2016 NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_provenance.
- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion SIO_000772 25218063 NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_provenance.
- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion evidence source_evidence_literature NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_provenance.
- NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_assertion description "[Our results thus expand the clinical phenotypes associated with biallellic STIL mutations to include holoprosencephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1219845.RAGPNQOySxfhTQ5FZJR14eCQcz5A0vy_dbBiNqJHqzNcM130_provenance.