Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion> ?p ?o ?g. }
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- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion type Assertion NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_head.
- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion description "[We identified an inherited brain-specific folate transport defect that is caused by mutations in the folate receptor 1 (FOLR1) gene coding for folate receptor alpha (FRalpha).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion evidence source_evidence_literature NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion SIO_000772 19732866 NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion wasDerivedFrom befree-20140225 NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_assertion wasGeneratedBy ECO_0000203 NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.