Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_assertion description "[Four (6%) of 72 patients with RA, 2 (13%) of 16 with OA, and 1 (8%) of 12 with other arthropathies harbored mutant H-ras proto-oncogenes, and were heterozygous at codon 13 for the GGT-->GAT (Gly-->Asp) change.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_assertion evidence source_evidence_literature NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_assertion SIO_000772 9324018 NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_assertion wasDerivedFrom befree-20140225 NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_assertion wasGeneratedBy ECO_0000203 NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP185069.RA3aeGZhWGvkMLPGIiw21xsdl8Lyr0qKhBvF-EBEfbzKw130_provenance.