Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP360859.RAkenbO6PvbIyFDfn5YX98Guw0dxFg4eKt0-CHCXcA9xo130_provenance.