Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_assertion description "[Clinical parameters can predict for mutation carriers and help prioritize gene testing to reduce costs in nonsyndromic pheochromocytoma presentations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_assertion evidence source_evidence_literature NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_assertion SIO_000772 19825962 NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_assertion wasDerivedFrom gad-20150221 NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_assertion wasGeneratedBy ECO_0000203 NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.
- gad-20150221 importedOn "2015-02-21" NP157958.RAa1iQeVmxpLqItR1vSHO1Iyis9rvDiLei0V7hK4SooLs130_provenance.