Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion> ?p ?o ?g. }
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- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion type Assertion NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_head.
- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion description "[Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion evidence source_evidence_literature NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion SIO_000772 15892853 NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion wasDerivedFrom befree-20140225 NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_assertion wasGeneratedBy ECO_0000203 NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.