Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion> ?p ?o ?g. }
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- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion type Assertion NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_head.
- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion description "[We further suggest that loss of necdin contributes to the neurological phenotype of PWS, and raise the possibility that co-deletion of necdin and the related protein Magel2 may explain the lack of single gene mutations in PWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.
- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion evidence source_evidence_literature NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.
- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion SIO_000772 15649943 NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.
- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion wasDerivedFrom befree-20150227 NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.
- NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_assertion wasGeneratedBy ECO_0000203 NP912040.RAaEqTNsdPvQGPyls6cyA9fZBwwHhAWB0hLfR3Q17MzD8130_provenance.