Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_assertion description "[In addition, we generated several stable cell lines expressing mutant barttins to clarify the consequence of the previously reported barttin mutations in Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_assertion evidence source_evidence_literature NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_assertion SIO_000772 12761627 NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_assertion wasDerivedFrom befree-2016 NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_assertion wasGeneratedBy ECO_0000203 NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.
- befree-2016 importedOn "2016-02-19" NP395257.RA3WEC43HR3ehOF46wCrTh3yaXlJyHUSYgTcjT7-w0u-w130_provenance.