Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion> ?p ?o ?g. }
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- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion type Assertion NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_head.
- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion description "[Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: the C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_provenance.
- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion evidence source_evidence_literature NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_provenance.
- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion SIO_000772 14583443 NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_provenance.
- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion wasDerivedFrom gad-20150221 NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_provenance.
- NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_assertion wasGeneratedBy ECO_0000203 NP82320.RAx3CDmqC9Gw3GdPZO6a17Mgh5kQ0v-WYghLwAQgzowu0130_provenance.