Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion description "[Taken together, these findings suggest that autosomal genes account for the majority of familial cases of KS, and that unique neuroendocrine phenotypes consistent with some GnRH neuronal migration may exist in these patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion evidence source_evidence_literature NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion SIO_000772 11297579 NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion wasDerivedFrom befree-2016 NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_assertion wasGeneratedBy ECO_0000203 NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.
- befree-2016 importedOn "2016-02-19" NP314017.RAV7BRUsoOdzU1RHxHT_3wVV8bKVnofKvgf8DIaZhMZBw130_provenance.