Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion> ?p ?o ?g. }
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- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion type Assertion NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_head.
- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion description "[In Albright hereditary osteodystrophy, heterozygous G(s)alpha null mutations only lead to PTH, TSH, and gonadotropin resistance when inherited maternally [pseudohypoparathyroidism type 1A; (PHP1A)].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion evidence source_evidence_literature NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion SIO_000772 12970307 NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion wasDerivedFrom befree-20140225 NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_assertion wasGeneratedBy ECO_0000203 NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.