Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion> ?p ?o ?g. }
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- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion type Assertion NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_head.
- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion description "[Germline mutations of PTPN11 are causative of Noonan syndrome and LEOPARD syndrome in humans in which there are recognized skeletal abnormalities that include growth retardation, spinal curvature and chest malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_provenance.
- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion evidence source_evidence_literature NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_provenance.
- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion SIO_000772 25178522 NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_provenance.
- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion wasDerivedFrom befree-2016 NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_provenance.
- NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_assertion wasGeneratedBy ECO_0000203 NP1215965.RA7ZJXUIYJyAldwzcgg9q-2uToHWbX9bnrJC9jVxtHOZ8130_provenance.