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- source_evidence_literature type ECO_0000212 NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_assertion wasGeneratedBy ECO_0000203 NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_assertion wasDerivedFrom befree-20150227 NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_assertion SIO_000772 10536986 NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_assertion evidence source_evidence_literature NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.
- NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_assertion description "[For example, mutations of the MITF gene cause Waardenburg syndrome type 2 (Tassabehji et al, 1994; Nobukuni et al, 1996) as well as Tietz syndrome (Smith et al, 1997).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557220.RA6TXs0b0Qh0PZ-77Ae_dPX5Ogq88jOGi5sjy2xZNJ_2M130_provenance.