Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_assertion description "[Applying the polymerase chain reaction (PCR) technique to exon 2 of the spectrin alpha I domain, we have established that the mutation responsible for spectrin Culoz is alpha I 40 Gly----Val; GGT----GTT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_assertion evidence source_evidence_literature NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_assertion SIO_000772 2384601 NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_assertion wasDerivedFrom befree-20140225 NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_assertion wasGeneratedBy ECO_0000203 NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.
- befree-20140225 importedOn "2014-02-25" NP466140.RAHjcsTvkowHq3p-fD2NRLEd-DTn0ua8G-3-hj6vIOE38130_provenance.