Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP766851.RA6N9AisbT8b_ug6hgBv2IdyPdac3Vrm-P-k93XyFoCgg130_provenance.