Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_assertion description "[We analyzed 3 polymorphisms, from codons 10 (TCT to TCC), 325 (CCC to CCG) and 594 (ACA to ACG) of ESRalpha, and a highly polymorphic dinucleotide repeat, D5S207, located within 200 kb of the GRL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_assertion evidence source_evidence_literature NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_assertion SIO_000772 11400122 NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_assertion wasDerivedFrom befree-20140225 NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_assertion wasGeneratedBy ECO_0000203 NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168023.RA2vVA9v2xEHQBVaiEVwQNqz5gs8l0b68ssGMjab6zNwU130_provenance.