Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_assertion description "[The MPZ gene Ser44Phe mutation found in the HMSN II family presented in this study suggests that genetic analysis of HMSN II families should also include the MPZ gene, previously not considered to be involved in the axonal form of HMSN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_assertion evidence source_evidence_literature NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_assertion SIO_000772 9595994 NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_assertion wasDerivedFrom befree-20150227 NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_assertion wasGeneratedBy ECO_0000203 NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568198.RAbaWXXMTxSxYzeBKsYQFD7PFtt0x8dRU7iUbTUlm9aLU130_provenance.