Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_assertion description "[Hereditary sensory neuropathy type I (HSN I) is an axonal form of autosomal-dominant hereditary motor and sensory neuropathy distinguished by prominent sensory loss that leads to painless injuries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_assertion evidence source_evidence_literature NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_assertion SIO_000772 21194679 NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_assertion wasDerivedFrom befree-2016 NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_assertion wasGeneratedBy ECO_0000203 NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP862308.RAZdSBarVLdqsTQl2_9JZAQfbBKndfCvqcPYxskMA3J_g130_provenance.