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- source_evidence_literature type ECO_0000212 NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_assertion description "[Double trouble in hereditary neuropathy: concomitant mutations in the PMP-22 gene and another gene produce novel phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_assertion evidence source_evidence_literature NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_assertion SIO_000772 16401743 NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_assertion wasDerivedFrom befree-20150227 NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_assertion wasGeneratedBy ECO_0000203 NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP632536.RAVh3sohOkdus2pDXDh19_Xj_EunBnqFoyaOmN2ZFi6d8130_provenance.