Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_assertion description "[Mutations in SOD1, ANG, VAPB, TARDBP and FUS genes have been identified in amyotrophic lateral sclerosis (ALS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_assertion evidence source_evidence_literature NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_assertion SIO_000772 20577002 NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_assertion wasDerivedFrom gad-20150221 NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_assertion wasGeneratedBy ECO_0000203 NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.
- gad-20150221 importedOn "2015-02-21" NP179618.RAvA7MN4fJxCQgwFHOWVlQB1S3p_YmptlTNuiAebj1aMc130_provenance.