Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_assertion description "[Mutations in the RAF1 are associated with Noonan syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_assertion evidence source_evidence_literature NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_assertion SIO_000772 19020799 NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_assertion wasDerivedFrom lhgdn-20090331 NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_assertion wasGeneratedBy ECO_0000203 NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP243885.RAP1nm_K5bfgKxZM-apy1yMcnvz5wg6GcDFDhruw3R3Mc130_provenance.