Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion> ?p ?o ?g. }
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- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion type Assertion NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_head.
- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion wasGeneratedBy ECO_0000203 NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_provenance.
- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion wasDerivedFrom befree-20140225 NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_provenance.
- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion SIO_000772 15082788 NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_provenance.
- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_assertion evidence source_evidence_literature NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_provenance.
- NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_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." NP692921.RAeuacam9-1OOEzXbRb7ZkYwVUVX828UJoiT_XGseuIcw130_provenance.