Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion> ?p ?o ?g. }
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- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion type Assertion NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_head.
- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_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." NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_provenance.
- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion evidence source_evidence_curated NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_provenance.
- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion SIO_000772 17603482 NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_provenance.
- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion wasDerivedFrom ctd_human-2016 NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_provenance.
- NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_assertion wasGeneratedBy ECO_0000218 NP20133.RAe1tm_g-6So2fXLTrHCRS-m-roA7xMr0gZv39xeu7Llw130_provenance.