Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_assertion description "[Based on the InSiGHT database and the original references that reported the mutations, we analyzed the distributions of MLH1 and MSH2 mutations in yellow race and white race respectively and compared them subsequently.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_assertion evidence source_evidence_literature NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_assertion SIO_000772 21155023 NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_assertion wasDerivedFrom befree-20140225 NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_assertion wasGeneratedBy ECO_0000203 NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP475022.RA2xZtE3p8mBet-zvOQfZ9BOJPWStoggo_3-0xY2vIza8130_provenance.