Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion> ?p ?o ?g. }
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- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion type Assertion NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_head.
- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion wasGeneratedBy ECO_0000203 NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_provenance.
- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion wasDerivedFrom lhgdn-20090331 NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_provenance.
- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion SIO_000772 17056636 NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_provenance.
- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion evidence source_evidence_literature NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_provenance.
- NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_assertion description "[Noonan syndrome affected individuals show heterozygous PTPN11 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186669.RA81QsoWeeTETO78CZ1UMR7bR5nzMoobEOT8TCdTFvQiI130_provenance.