Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_assertion description "[CAST-PCR gave rapid and accurate results for the common V600E and V600K mutations, however additional assays are required to detect rarer BRAF mutation types found in 3-4% of melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_assertion evidence source_evidence_literature NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_assertion SIO_000772 23584600 NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_assertion wasDerivedFrom befree-2016 NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_assertion wasGeneratedBy ECO_0000203 NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1069142.RARYWqv3w11b3I_V9sRkWmgxHDFuoCxV5Sasi5aSWLlW4130_provenance.