Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP233752.RAI22xAzikQ91I7Po_LNCsGyTjTOqZD79oIW43sulyDPw130_provenance.