Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion evidence source_evidence_literature NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion SIO_000772 15024693 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion wasDerivedFrom befree-2016 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion wasGeneratedBy ECO_0000203 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- befree-2016 importedOn "2016-02-19" NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.