Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- befree-2016 importedOn "2016-02-19" NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_assertion wasGeneratedBy ECO_0000203 NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_assertion wasDerivedFrom befree-2016 NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_assertion SIO_000772 19822806 NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_assertion evidence source_evidence_literature NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.
- NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_assertion description "[NOS1AP is a genetic modifier of the long-QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768957.RAepjaVC_dZz9eKDuOjoBTT4gZ0Sq80VpfVx6QqUNRVNw130_provenance.