Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion> ?p ?o ?g. }
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- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion type Assertion NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_head.
- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion description "[Hereditary folate malabsorption is a rare, autosomal recessive disorder of proton-coupled folate transporter deficiency resulting in folate deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_provenance.
- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion evidence source_evidence_literature NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_provenance.
- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion SIO_000772 24534056 NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_provenance.
- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion wasDerivedFrom befree-2016 NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_provenance.
- NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_assertion wasGeneratedBy ECO_0000203 NP1155942.RAYcwfmB6UkGBu-P--w6H6lFHW3Li8E6tLuts2Kc92VlU130_provenance.