Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion> ?p ?o ?g. }
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- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion type Assertion NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_head.
- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion description "[Germline ASXL1 mutations occur in patients with Bohring-Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_provenance.
- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion evidence source_evidence_literature NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_provenance.
- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion SIO_000772 24218140 NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_provenance.
- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion wasDerivedFrom befree-20150227 NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_provenance.
- NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_assertion wasGeneratedBy ECO_0000203 NP978660.RAIcuIHjLqp1GpRFJlOE0fpwpzm8pTWJZHgaR0U3NhI7w130_provenance.