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- source_evidence_literature type ECO_0000212 NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_assertion evidence source_evidence_literature NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_assertion SIO_000772 10852374 NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_assertion wasDerivedFrom befree-20150227 NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_assertion wasGeneratedBy ECO_0000203 NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP693623.RAjAlJXgNkLiZWCYm22oxCREgBqmbypFcTgMc-su6_cIg130_provenance.