Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion> ?p ?o ?g. }
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- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion type Assertion NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_head.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion description "[This is the first report of the molecular basis of prothrombin deficiency in Indian patients and we suggest the eponym 'Prothrombin Vellore 1' for Ala362 --> Thr mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion evidence source_evidence_literature NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion SIO_000772 15892853 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion wasDerivedFrom befree-20150227 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.
- NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_assertion wasGeneratedBy ECO_0000203 NP389970.RAO-IDCNCX_mtJKp9-PqwBMvHVH8NErWvp6cZXC_EQUIU130_provenance.