Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_assertion description "[Mutation analysis was performed in 28 patients with EI by direct sequencing of KRT1 and KRT10 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_assertion evidence source_evidence_literature NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_assertion SIO_000772 21271994 NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_assertion wasDerivedFrom befree-2016 NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_assertion wasGeneratedBy ECO_0000203 NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP868177.RAyOBw1mkXfu28EYyoKpAX-1TyrX6HoB1kI2k2EiFOcdQ130_provenance.