Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion> ?p ?o ?g. }
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- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion type Assertion NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_head.
- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion description "[The spectrum of mutations in the PCFT gene, coding for an intestinal folate transporter, that are the basis for hereditary folate malabsorption.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_provenance.
- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion evidence source_evidence_curated NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_provenance.
- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion SIO_000772 17446347 NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_provenance.
- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion wasDerivedFrom ctd_human-20130708 NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_provenance.
- NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_assertion wasGeneratedBy ECO_0000218 NP29976.RAwyy_bp9pYTp97GMWtz7Sbp6aJu8q8Bf3O8irvMKL_30130_provenance.