Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_assertion wasGeneratedBy ECO_0000203 NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_assertion wasDerivedFrom befree-20140225 NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_assertion SIO_000772 21098271 NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_assertion evidence source_evidence_literature NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_assertion description "[Other frequent abnormalities included whole-chromosome uniparental isodisomies (wUPIDs) 9 and 11, gain of 17q not associated with isochromosome formation, extra gain of part of 21q, deletions of ETS variant 6 (ETV6), cyclin-dependent kinase inhibitor 2A (CKDN2A) and paired box 5 (PAX5), and PAN3 poly(A) specific ribonuclease subunit homolog (PAN3) microdeletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP840498.RA1HpYwuzYpFTQWLqgjGEdmPcenCJNduh_e_5vKGY6VMc130_provenance.