Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion> ?p ?o ?g. }
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- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion type Assertion NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_head.
- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion description "[Germline gain-of-function mutations in RAF1 cause Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_provenance.
- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion evidence source_evidence_curated NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_provenance.
- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion SIO_000772 17603482 NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_provenance.
- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion wasDerivedFrom ctd_human-20130708 NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_provenance.
- NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_assertion wasGeneratedBy ECO_0000218 NP21176.RAhcuefXaibpI1k69yQBKiKl-cbOQ6nqs-mmG1m_AIs_Q130_provenance.