Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_assertion description "[Oncogenic gain-of-function mutations in NOTCH1 commonly occur in human T-cell lymphoblastic leukemia/lymphoma and B-cell chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_assertion evidence source_evidence_literature NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_assertion SIO_000772 22006338 NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_assertion wasDerivedFrom befree-20140225 NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_assertion wasGeneratedBy ECO_0000203 NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP628090.RAeo95_CYy0F645wcyn-Fpg-Y56VdksOaCIQ97QvSFiOQ130_provenance.