Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion description "[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion evidence source_evidence_literature NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion SIO_000772 10090952 NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion wasDerivedFrom befree-2016 NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_assertion wasGeneratedBy ECO_0000203 NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.
- befree-2016 importedOn "2016-02-19" NP248434.RA5sDPx57P2m2QFrAsM8NvBvwcJKb9e_FYOBhqB14Nwho130_provenance.