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- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion type Assertion NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_head.
- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion wasGeneratedBy ECO_0000203 NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_provenance.
- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion wasDerivedFrom befree-20150227 NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_provenance.
- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion SIO_000772 22310223 NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_provenance.
- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion evidence source_evidence_literature NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_provenance.
- NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_assertion description "[Clinical molecular diagnostic centers routinely screen SHH, ZIC2, SIX3 and TGIF for mutations that can help to explain holoprosencephaly and related brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694808.RAW60EQ32yCVmoP37ivL-OzWvdd70FxpM8cHb5xro5_7Y130_provenance.