Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_assertion description "[Moreover, this mechanism of action mimicked the effects of overexpression of the Ras-GAP domain of neurofibromin, GAP-related domain (GRD) I, which is part of the upstream mechanism for regulation of Ras activation and a PKC-alpha substrate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_assertion evidence source_evidence_literature NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_assertion SIO_000772 16635257 NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_assertion wasDerivedFrom befree-20140225 NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_assertion wasGeneratedBy ECO_0000203 NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625987.RAx91B0P-In-hjp1D0jH24tKHya81AlbPOYyyy2t2daPs130_provenance.