Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_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." NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_assertion evidence source_evidence_literature NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_assertion SIO_000772 11030761 NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_assertion wasDerivedFrom befree-20140225 NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_assertion wasGeneratedBy ECO_0000203 NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP417680.RAfn5iPmPXUZjmlvePqWeJ4nH92TIP9uQ9lFRKR_VTYQA130_provenance.