Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_assertion description "[No marker chromosome 1, homogeneously staining region (HSR), or double minutes (DMS) was observed in these patients, all of which have been previously reported in advanced neuroblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_assertion evidence source_evidence_literature NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_assertion SIO_000772 2704332 NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_assertion wasDerivedFrom befree-20140225 NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_assertion wasGeneratedBy ECO_0000203 NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.
- befree-20140225 importedOn "2014-02-25" NP240407.RATzMyBlqdHfSxKwjzSwOWHLn0Hp7HRO-pauiPIccy9Ns130_provenance.