Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_assertion description "[Most importantly, we discovered that TRRAP harbored a recurrent mutation that clustered in one position (p. Ser722Phe) in 6 out of 167 affected individuals (?4%), as well as a previously unidentified gene, GRIN2A, which was mutated in 33% of melanoma samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_assertion evidence source_evidence_literature NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_assertion SIO_000772 21499247 NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_assertion wasDerivedFrom befree-2016 NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_assertion wasGeneratedBy ECO_0000203 NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.
- befree-2016 importedOn "2016-02-19" NP887709.RAHDKt2abpzSiLeMV2JnHCiZRlbghyzt2biAtOZPYVQLI130_provenance.