Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion> ?p ?o ?g. }
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- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion type Assertion NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_head.
- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion description "[Neurofibromatosis type 1 (NF1), a common autosomal dominant disorder caused by mutations of the NF1 gene, is characterized by multiple neurofibromas, pigmentation anomalies, and a variety of other possible complications, including an increased risk of malignant neoplasias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_provenance.
- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion evidence source_evidence_literature NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_provenance.
- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion SIO_000772 10677298 NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_provenance.
- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion wasDerivedFrom befree-20140225 NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_provenance.
- NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_assertion wasGeneratedBy ECO_0000203 NP536811.RAXnyC46QgpRqC_7RjBX4PUYWPqbHBBG-mUAK0AkeVEQ0130_provenance.