Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_assertion description "[Of these 12 patients, three had homozygous G701D/G701D and heterozygous Hb E; one compound heterozygous SAO/G701D and heterozygous alpha(+)-thalassemia; and one compound heterozygous G701D/A858D and heterozygous Hb E. Of 6 patients without SLC4A1 mutation, two each carried heterozygous or homozygous Hb E and one of the latter also had Hb H disease (--(SEA)/-alpha(4.2)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_assertion evidence source_evidence_literature NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_assertion SIO_000772 18266205 NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_assertion wasDerivedFrom befree-20150227 NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_assertion wasGeneratedBy ECO_0000203 NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP480994.RAcGoAQn7f4k95FI_FuZZ45KBRJb7lINJD_UsJiJ79LZU130_provenance.