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- source_evidence_literature type ECO_0000212 NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_assertion wasGeneratedBy ECO_0000203 NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_assertion wasDerivedFrom befree-20140225 NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_assertion SIO_000772 10845668 NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_assertion evidence source_evidence_literature NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_assertion description "[The aim of our study was to investigate HFE mutations in patients with HCC in NCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.
- befree-20140225 importedOn "2014-02-25" NP207974.RA6wM4X7b421PySUo1aHBW1oLf4K5Jz0ZjwFhhsKEQf1s130_provenance.