Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_assertion description "[Mutations in the C-terminal half of MID1, an RBCC (RING, B-box and coiled-coil) protein, have recently been shown to underlie the X-linked form of OS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_assertion evidence source_evidence_literature NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_assertion SIO_000772 11030761 NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_assertion wasDerivedFrom befree-20140225 NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_assertion wasGeneratedBy ECO_0000203 NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP664985.RAdlZ_R5ajFbGeyD3P1XVUiku_uSwBQhVZ2-kwrNF3Jjs130_provenance.