Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion> ?p ?o ?g. }
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- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion type Assertion NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_head.
- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_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." NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion evidence source_evidence_literature NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion SIO_000772 17446347 NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion wasDerivedFrom befree-20140225 NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_assertion wasGeneratedBy ECO_0000203 NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.