Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion> ?p ?o ?g. }
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- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion type Assertion NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_head.
- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_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." NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_provenance.
- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion evidence source_evidence_literature NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_provenance.
- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion SIO_000772 10447258 NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_provenance.
- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion wasDerivedFrom befree-20140225 NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_provenance.
- NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_assertion wasGeneratedBy ECO_0000203 NP790265.RAIX3uUWdubAl_uxkCEEsKT_tpgWQIMCxneBp1VXKvUJU130_provenance.