Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_assertion description "[Limb-girdle muscular dystrophy type 2A (LGMD2A) due to mutations in the CAPN3 gene is one of the most common of autosomal recessive limb-girdle muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_assertion evidence source_evidence_literature NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_assertion SIO_000772 24715573 NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_assertion wasDerivedFrom befree-2016 NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_assertion wasGeneratedBy ECO_0000203 NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1171739.RAglwl-fpSbczmL-SxkK1u6v5gKul73QtS42Y9-3ev3N8130_provenance.