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- source_evidence_literature type ECO_0000212 NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_assertion description "[Alterations of known genes in PRCC include missense mutations in the MET oncogene (7q31) and rare translocations fusing TFE3 at Xp11.2 with a variety of other loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_assertion evidence source_evidence_literature NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_assertion SIO_000772 12213728 NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_assertion wasDerivedFrom befree-2016 NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_assertion wasGeneratedBy ECO_0000203 NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.
- befree-2016 importedOn "2016-02-19" NP366941.RA3Vv6KmWbSHewM0l01hk8R7RCRBmIiqVdY6PlfOXykgM130_provenance.