Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP221853.RAHVbCWPcgPIY6Nq5tVvDtHc1J1nu5RqBw-ATOxNwYeJs130_provenance.