Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_assertion description "[Molecular alterations of p73 in human esophageal squamous cell carcinomas: loss of heterozygosity occurs frequently; loss of imprinting and elevation of p73 expression may be related to defective p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_assertion evidence source_evidence_literature NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_assertion SIO_000772 10753204 NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_assertion wasDerivedFrom befree-2016 NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_assertion wasGeneratedBy ECO_0000203 NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.
- befree-2016 importedOn "2016-02-19" NP280317.RAEarMCzxWEB8tDijZ0jawVZYsRvXBzPOWSBE72X2ceoU130_provenance.