Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_assertion description "[Based on these observations, an autosomal dominant form of ectrodactyly is assumed to reside in this region and the locus has been designated SHFD1 (split hand/split foot disorder).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_assertion evidence source_evidence_literature NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_assertion SIO_000772 7987314 NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_assertion wasDerivedFrom befree-20150227 NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_assertion wasGeneratedBy ECO_0000203 NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.
- befree-20150227 importedOn "2015-02-27" NP787199.RA11FFlTaHr5w0KHEBChgHljTuCguBGi3azsXN4lqH0ko130_provenance.