Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_assertion description "[The deletion breakpoints were precisely identified for each deletion and primers were designed in the unique regions across the breakpoints of HPFH-1 (Black), HPFH-2 (Ghanaian), HPFH-3 (Asian Indian), HPFH-4 (Italian), HPFH-5 (Italian), HPFH-6 (Vietnamese), HPFH-7 (Kenyan), and SEA-HPFH (Southeast Asian).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_assertion evidence source_evidence_literature NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_assertion SIO_000772 16271016 NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_assertion wasDerivedFrom befree-20150227 NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_assertion wasGeneratedBy ECO_0000203 NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.
- befree-20150227 importedOn "2015-02-27" NP463983.RASHvrDF17N3wu1kMBF7U_KVGyEN--P_2iOYExUZbCe9A130_provenance.