Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP353544.RAAC70Q0KbPguPUR9gKidPIjRqaN1JXWmr2VVv_RlR0nc130_provenance.