Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion> ?p ?o ?g. }
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- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion type Assertion NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_head.
- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion description "[We also screened 408 sporadic patients with CHDs and identified a case with ASD and a 17-bp deletion in ACTC1 predicting a non-functional protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion evidence source_evidence_literature NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion SIO_000772 17947298 NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion wasDerivedFrom befree-20150227 NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_assertion wasGeneratedBy ECO_0000203 NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.