Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_assertion description "[Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency are autosomal recessive inborn errors of metabolism with severe neurological symptoms resulting from a lack of sulfite oxidase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_assertion evidence source_evidence_literature NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_assertion SIO_000772 12533804 NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_assertion wasDerivedFrom befree-2016 NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_assertion wasGeneratedBy ECO_0000203 NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.
- befree-2016 importedOn "2016-02-19" NP380667.RAuJnzOcblKIFFfFJ0ERFHBY0wU6n3KYyZP5LLf4n8_F4130_provenance.