Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_assertion description "[At presentation, 93 % of cases of AML (8 of 8 M1, 10 of 11 M2, 2 of 2 M4, 5 of 6 M5, and 2 of 2 M6; French-American-British classification system) showed p15 methylation, but none showed p16 methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_assertion evidence source_evidence_literature NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_assertion SIO_000772 11413509 NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_assertion wasDerivedFrom befree-2016 NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_assertion wasGeneratedBy ECO_0000203 NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.
- befree-2016 importedOn "2016-02-19" NP321367.RApIB5Z1U68vdmvecmuCKnxANxzFRmK2DKipdqvn2I93o130_provenance.