Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_assertion description "[Chromosomal features of CHP-382/JK shared with other neuroblastoma cell lines were the deletion of 1p and the presence of extra 17q material.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_assertion evidence source_evidence_literature NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_assertion SIO_000772 2582423 NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_assertion wasDerivedFrom befree-20150227 NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_assertion wasGeneratedBy ECO_0000203 NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978738.RAcATWEDg72eTAlKq5KDeLLWhRR63Vxs1PtB0hBWcP0cY130_provenance.