Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_assertion description "[Our findings on rhabdomyosarcoma samples showed multiple copy number alterations in chromosome regions implicated in malignancy progression and indicated a strong expression of MAP2K4 and MCL1 genes, both involved in different biological functions of complicated signalling pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_assertion evidence source_evidence_literature NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_assertion SIO_000772 19012245 NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_assertion wasDerivedFrom befree-20150227 NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_assertion wasGeneratedBy ECO_0000203 NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP690559.RAnXUA22DsNKOLkaO4yl5Ew1TbVX47hjMgyH-dGpHcp2g130_provenance.