Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_assertion description "[The identification of a novel missense mutation in only one of the patients implied that TCF8 does not play a significant role in the pathogenesis of FECD in this Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_assertion evidence source_evidence_literature NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_assertion SIO_000772 18172091 NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_assertion wasDerivedFrom befree-2016 NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_assertion wasGeneratedBy ECO_0000203 NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP647992.RANALCVk1A-HXrGM6BeqwOOHjK2VKlsG_zrFDaD9Jmh6Q130_provenance.