Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_assertion wasGeneratedBy ECO_0000203 NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_assertion wasDerivedFrom befree-20150227 NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_assertion SIO_000772 15082788 NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_assertion evidence source_evidence_literature NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.
- NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_assertion description "[Recently, human NDRG1 was identified as a gene responsible for hereditary motor and sensory neuropathy-Lom (classified as Charcot-Marie-Tooth disease type 4D), which is characterized by early-onset peripheral neuropathy, leading to severe disability in adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842609.RAIfV9Lq7iPPXbRhFWgEBJenL-KXfyHY8qLtgfuQntCF8130_provenance.