Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_assertion description "[This case-control study was designed for mutational analysis of the GDF9 coding region in a cohort of women with premature ovarian failure (n = 127), primary amenorrhea (n = 58), and secondary amenorrhea (n = 10) compared with controls (n = 220).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_assertion evidence source_evidence_literature NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_assertion SIO_000772 16278619 NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_assertion wasDerivedFrom befree-2016 NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_assertion wasGeneratedBy ECO_0000203 NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.
- befree-2016 importedOn "2016-02-19" NP521927.RA3JeNjl41RQw3SZPLa_EfcjhcP8AQCe2C3BT0r3OXSZc130_provenance.