Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_assertion description "[ARHGEF17 showed a G1865A mutation leading to W622X in a cell line derived from a mucosal melanoma; in RB1 a C1411T base change resulting in Q471X was discovered in a cell line derived from an acral melanoma; and the FGFR3 and DENND2D genes had intronic insertions leading to PTCs in cell lines derived from superficially spreading melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_assertion evidence source_evidence_literature NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_assertion SIO_000772 18677770 NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_assertion wasDerivedFrom befree-20140225 NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_assertion wasGeneratedBy ECO_0000203 NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP424712.RA4q1FMIQ66aIfU2iQVWNmddCGvbNEZQaqIQ3wNBn6HSY130_provenance.