Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion> ?p ?o ?g. }
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- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion type Assertion NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_head.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_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." NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion evidence source_evidence_literature NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion SIO_000772 15892853 NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion wasDerivedFrom befree-20150227 NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.
- NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_assertion wasGeneratedBy ECO_0000203 NP389687.RA7Ow6IKam45K5bPvHa68zoQMiD4cIK3pWpmhP5xskGOY130_provenance.