Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_assertion description "[Although hidden genetic changes have been found in some trisomies, for example, mutations in KIT in acute myelocytic leukemia (AML) with +4 and in MET in hereditary papillary kidney carcinoma with trisomy 7, none associated with +8 have so far been discovered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_assertion evidence source_evidence_literature NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_assertion SIO_000772 12550762 NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_assertion wasDerivedFrom befree-2016 NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_assertion wasGeneratedBy ECO_0000203 NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.
- befree-2016 importedOn "2016-02-19" NP381581.RAU1M-R450Ip7z6EJcDXlGjNYX9S5NtY1BJY1CeaR2-hk130_provenance.