Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_assertion description "[A 27 base-pair deletion of the anti-mllerian type II receptor gene is the most common cause of the persistent mllerian duct syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_assertion evidence source_evidence_curated NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_assertion SIO_000772 8872466 NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_assertion wasDerivedFrom uniprot-20130724 NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_assertion wasGeneratedBy ECO_0000218 NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP376.RA6WknTe-hsTKZ4ipGBzy60UnFnyckYpOyOzzIqmsrhjw130_provenance.