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- source_evidence_literature type ECO_0000212 NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_assertion description "[Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_assertion evidence source_evidence_literature NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_assertion SIO_000772 16107578 NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_assertion wasDerivedFrom befree-2016 NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_assertion wasGeneratedBy ECO_0000203 NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.
- befree-2016 importedOn "2016-02-19" NP509431.RAQCumUA4MUrdd9KjV48DlUc2je_E4QiDt1eJjORUdCCE130_provenance.