Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion> ?p ?o ?g. }
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- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion type Assertion NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_head.
- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion description "[Beckwith-Wiedemann syndrome (BWS, OMIM 130650) is characterized by macrosomia, macroglossia, visceromegaly, hemihypertrophy, abdominal wall defects, ear creases/pits, neonatal hypoglycemia, polyhydramnios, placentomegaly, placental mesenchymal dysplasia, cardiac defects, nevus flammeus, hemangiomata, and an increased frequency of embryonal tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion evidence source_evidence_literature NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion SIO_000772 17638616 NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion wasDerivedFrom befree-20140225 NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_assertion wasGeneratedBy ECO_0000203 NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.