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- source_evidence_literature type ECO_0000212 NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_assertion description "[In a French family, we have identified a splicing mutation in the SCN5A gene leading to hereditary progressive cardiac conduction defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_assertion evidence source_evidence_literature NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_assertion SIO_000772 12598077 NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_assertion wasDerivedFrom befree-20150227 NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_assertion wasGeneratedBy ECO_0000203 NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP683216.RA5PNrkGs-3lymACnON6KGcLobyuZctU8IPxp3pP_x4cQ130_provenance.