Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion> ?p ?o ?g. }
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- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion type Assertion NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_head.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion description "[Exome sequencing identifies WDR35 variants involved in Sensenbrenner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion evidence source_evidence_literature NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion SIO_000772 20817137 NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion wasDerivedFrom befree-20150227 NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.
- NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_assertion wasGeneratedBy ECO_0000203 NP931589.RAA9l6XWcLFFRQFsiJNNWVh2kUM1JVp1S7yF37yI6p7jo130_provenance.