Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_assertion description "[The syndrome o SEDT, precocious OA, and brachydactyly in a kindred of Chiloe Islanders is associated with a point mutation in 1 allele of the COL2A1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_assertion evidence source_evidence_literature NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_assertion SIO_000772 8024616 NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_assertion wasDerivedFrom befree-20140225 NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_assertion wasGeneratedBy ECO_0000203 NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP670026.RA1itm5y3Zqi3_PkvHdfqCxkvxg0hQ05AHzVsNjff2Euw130_provenance.