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- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion type Assertion NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_head.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion description "[Functional analysis of a novel GATA3 mutation in a family with the hypoparathyroidism, deafness, and renal dysplasia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion evidence source_evidence_literature NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion SIO_000772 15705923 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion wasDerivedFrom befree-20150227 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.
- NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_assertion wasGeneratedBy ECO_0000203 NP419368.RA7KNNHT0_5zBFWX0oal2iucbwYiHvFllfGukoTsvFqU8130_provenance.