Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_assertion description "[In this report we present clinical, cytogenetic, and molecular-cytogenetic data of a patient with ambiguous genitalia and true hermaphroditism, who had a unique mosaic karyotype, comprising three different cell lines: 46,XX(SRY+), 45,X(SRY+), and 45,X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_assertion evidence source_evidence_literature NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_assertion SIO_000772 12503111 NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_assertion wasDerivedFrom befree-2016 NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_assertion wasGeneratedBy ECO_0000203 NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.
- befree-2016 importedOn "2016-02-19" NP378877.RAoXSd5ed2u6R3i0IvKikTZKHQ4HUf3ViFIN5uturuihc130_provenance.