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- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion type Assertion NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_head.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion wasGeneratedBy ECO_0000203 NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion wasDerivedFrom befree-20140225 NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion SIO_000772 19878917 NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion evidence source_evidence_literature NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.
- NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_assertion description "[Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP666509.RA6MeXfOSQnE2pWKxHmRp00wZX2eMqglWkK9dqon3MCXw130_provenance.