Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion> ?p ?o ?g. }
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- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion type Assertion NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_head.
- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion wasGeneratedBy ECO_0000203 NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_provenance.
- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion wasDerivedFrom befree-20150227 NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_provenance.
- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion SIO_000772 15082788 NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_provenance.
- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_assertion evidence source_evidence_literature NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_provenance.
- NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_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." NP842615.RAcW-lpLEueTpaavMNos7fATA7jMwtSsrIWy494g34FRg130_provenance.