Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion> ?p ?o ?g. }
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- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion type Assertion NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_head.
- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion wasGeneratedBy ECO_0000203 NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_provenance.
- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion wasDerivedFrom lhgdn-20090331 NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_provenance.
- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion SIO_000772 17056636 NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_provenance.
- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion evidence source_evidence_literature NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_provenance.
- NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_assertion description "[Noonan syndrome affected individuals show heterozygous PTPN11 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220397.RA1V72dw9wlL1ozZ6nGbKrhr-owL-KPogtlNd2PKzeFJw130_provenance.