Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_assertion description "[A novel GNAS1 mutation, R201G, in McCune-albright syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_assertion evidence source_evidence_curated NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_assertion SIO_000772 10571700 NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_assertion wasDerivedFrom uniprot-20130724 NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_assertion wasGeneratedBy ECO_0000218 NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2836.RAx56_h07nMWd4Pr1lFeOni0plu3kjgHd0TNwbGZaMjVA130_provenance.