Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_assertion description "[Metachromatic leukodystrophy (MLD) is an inherited demyelinating disorder caused by the deficiency of arylsulphatase A (ASA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_assertion evidence source_evidence_literature NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_assertion SIO_000772 15326627 NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_assertion wasDerivedFrom befree-20140225 NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_assertion wasGeneratedBy ECO_0000203 NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513343.RAW-96VntIA6ljc98vfLEDPxFHOTwEupIS5vNMqM-pQ4Y130_provenance.