Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_assertion description "[p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_assertion evidence source_evidence_literature NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_assertion SIO_000772 11479205 NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_assertion wasDerivedFrom befree-20140225 NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_assertion wasGeneratedBy ECO_0000203 NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP507775.RA868RfF8Vm3VU1ijYI-PstLVPY-GxO74TJ7WjKGsTZLw130_provenance.