Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_assertion description "[Seven unrelated patients with hemoglobin (Hb) H disease and 27 individuals with alpha-chain structural alterations were studied to identify the alpha-globin gene mutations present in the population of Southeast Brazil.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_assertion evidence source_evidence_literature NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_assertion SIO_000772 10973135 NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_assertion wasDerivedFrom befree-2016 NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_assertion wasGeneratedBy ECO_0000203 NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.
- befree-2016 importedOn "2016-02-19" NP294115.RAl3wgPOakH7V4M1cMeBRtpMMjXVwumQ4XcdP2mg_20AU130_provenance.