Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion description "[MYH9-associated disorders (May-Hegglin anomaly, Epstein and Fechtner syndrome, and others) are inherited in an autosomal dominant manner and characterized by defects in different organs (including eyes, ears, kidneys and thrombocytes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion evidence source_evidence_literature NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion SIO_000772 23144074 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion wasDerivedFrom befree-20140225 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_assertion wasGeneratedBy ECO_0000203 NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP484831.RAwZEGThhhYWWWaRX_a1DQ4jP5t8RwvBKb_w3SLrWVkxc130_provenance.