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- source_evidence_literature type ECO_0000212 NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion description "[The peripheral myelin protein 22 mutation W28R was associated with CMT1 and profound deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion evidence source_evidence_literature NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion SIO_000772 11835375 NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion wasDerivedFrom befree-20140225 NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_assertion wasGeneratedBy ECO_0000203 NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP649662.RAANtA6S-Je33iz7Wmq1TiSI_8NDlNi5Kvh66H3aqvgaQ130_provenance.