Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_assertion description "[Two patients had paired mutations in the MVK gene (genotypes V377I/V377I and V377I/S135L) and displayed typical features of BD and MKD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_assertion evidence source_evidence_literature NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_assertion SIO_000772 17213252 NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_assertion wasDerivedFrom befree-2016 NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_assertion wasGeneratedBy ECO_0000203 NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.
- befree-2016 importedOn "2016-02-19" NP587991.RAujdkkGJ5toZbQO5GYN7A4xi_GWv9wva4e2oqz5n5oJI130_provenance.