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- source_evidence_literature type ECO_0000212 NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_assertion wasGeneratedBy ECO_0000203 NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_assertion wasDerivedFrom befree-20150227 NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_assertion SIO_000772 14553950 NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_assertion evidence source_evidence_literature NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.
- NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_assertion description "[Allelic loss of 13q14 was observed in 63.2% patients, most of them showing D13S319 and D13S25 deletion; 11% of patients showed TP53 monosomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790544.RAEL_z7btoP6mPywgzlgE-_zh9LN4Bx1IJ_Uk21nEm-Qo130_provenance.