Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_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." NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_assertion evidence source_evidence_literature NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_assertion SIO_000772 18172091 NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_assertion wasDerivedFrom befree-20150227 NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_assertion wasGeneratedBy ECO_0000203 NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP725872.RAm7u4eCruCW8hZBhPWsMBVeY3fp4SLpkhFdrg0ICP7Nc130_provenance.