Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_assertion description "[These results demonstrate that Japanese P4.2-deficiency is closely associated with the P4.2 gene and does not arise secondarily to a defect in another membrane protein, and further suggest that the P4.2-deficiency is related to the pathogenesis of the hemolytic anemia in this variant form of recessively inherited spherocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_assertion evidence source_evidence_literature NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_assertion SIO_000772 1558976 NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_assertion wasDerivedFrom befree-20140225 NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_assertion wasGeneratedBy ECO_0000203 NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477822.RAch_dvMEf6ptaA05ddTYP-rdZCkE95fGAhpwHlepxuDo130_provenance.