Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_assertion description "[Identification of a common PEX1 mutation in Zellweger syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_assertion evidence source_evidence_curated NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_assertion SIO_000772 10447258 NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_assertion wasDerivedFrom ctd_human-2016 NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_assertion wasGeneratedBy ECO_0000218 NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.
- ctd_human-2016 importedOn "2016-01-25" NP10438.RAod7FzWPNJVNg8_iMWmSfpxKQtbnpcGOV2bPH0a25dyc130_provenance.