Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_assertion description "[Complement factor H deficiency and endocapillary glomerulonephritis due to paternal isodisomy and a novel factor H mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_assertion evidence source_evidence_literature NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_assertion SIO_000772 21270828 NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_assertion wasDerivedFrom befree-20150227 NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_assertion wasGeneratedBy ECO_0000203 NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446501.RAb5pnX12mVipMCy6Vwz1filNKw6Cmwer5ZOfyobqejho130_provenance.