Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_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." NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_assertion evidence source_evidence_literature NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_assertion SIO_000772 17638616 NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_assertion wasDerivedFrom befree-20150227 NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_assertion wasGeneratedBy ECO_0000203 NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.
- befree-20150227 importedOn "2015-02-27" NP983417.RALh6UUoKBeUX1DM5KyVRY7txOPvdtmPQNRAdbdUNkZis130_provenance.