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- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion type Assertion NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_head.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion description "[Two novel disease-causing mutations in the CLRN1 gene in patients with Usher syndrome type 3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion evidence source_evidence_literature NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion SIO_000772 23304067 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion wasDerivedFrom befree-20150227 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.
- NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_assertion wasGeneratedBy ECO_0000203 NP1004854.RAzW33v-5G8J5-fcCDxy-QvlY9zTC-HmUBfDDSj-afT6U130_provenance.