Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_assertion description "[The two most common forms of X-linked adrenoleukodystrophy (X-ALD) are the cerebral forms (CER) with an inflammatory demyelinating reaction that resembles multiple sclerosis, and adrenomyeloneuropathy (AMN) which involves primarily the spinal cord and in which the inflammatory reaction is mild or absent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_assertion evidence source_evidence_literature NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_assertion SIO_000772 9143252 NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_assertion wasDerivedFrom befree-20140225 NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_assertion wasGeneratedBy ECO_0000203 NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.
- befree-20140225 importedOn "2014-02-25" NP939985.RAcTBu0yTsFFbxTe8W0dZBzwqDOP7isjPkXp8diyuuCro130_provenance.