Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP749128.RA5nqIpbUolivdKV2MCW9ahoX0WRXooK80bSP2DZ4MmiA130_provenance.