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- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion type Assertion NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_head.
- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion wasGeneratedBy ECO_0000218 NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_provenance.
- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion wasDerivedFrom uniprot-2016 NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_provenance.
- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion SIO_000772 10602116 NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_provenance.
- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion evidence source_evidence_curated NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_provenance.
- NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_assertion description "[Pendred syndrome: phenotypic variability in two families carrying the same PDS missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP539.RADXn1S8Cs36HifWShlf7wY5ApG3SqsPusbUs-L4H96Gw130_provenance.