Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion> ?p ?o ?g. }
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- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion type Assertion NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_head.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_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." NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion evidence source_evidence_literature NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion SIO_000772 15649943 NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion wasDerivedFrom befree-2016 NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.
- NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_assertion wasGeneratedBy ECO_0000203 NP476207.RAahxI2VTOloQT59U4SN3A8u2c4b9Bw_L7gO14As23-7c130_provenance.