Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_assertion description "[Mutations in the p63 gene have recently been delineated as the molecular basis for some cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an autosomal dominant disorder (MIM 129900).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_assertion evidence source_evidence_literature NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_assertion SIO_000772 11012604 NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_assertion wasDerivedFrom befree-20150227 NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_assertion wasGeneratedBy ECO_0000203 NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP857280.RAON9kJKgv_qRKyEbcCU0RB1UhQZ5WiA9MPA7_otke0Bo130_provenance.