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- source_evidence_literature type ECO_0000212 NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion description "[We suggest that these features, in particular severe developmental delay and epilepsy, may form part of the characteristic phenotype resulting from deletion of both FMR1 and FMR2 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion evidence source_evidence_literature NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion SIO_000772 10424820 NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion wasDerivedFrom befree-20150227 NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_assertion wasGeneratedBy ECO_0000203 NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412432.RAajw0Rh4g1-XcBG18m_vzVNh6YN8m8wnnYuizMbhZpt0130_provenance.