Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion description "[Although fibroblast growth factor-8 (FGF8) mutations have mainly found in patients with Kallmann syndrome, mice with a hypomorphic Fgf8 allele or complete gene invalidation display, aside from gonadotropin-releasing hormone deficiency, parts or even the entire spectrum of human VATER/VACTERL association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion evidence source_evidence_literature NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion SIO_000772 25131394 NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion wasDerivedFrom befree-2016 NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_assertion wasGeneratedBy ECO_0000203 NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1211443.RAj-GgbDEAQX7AR--lSBSozSr1-r_IF45ehZwzS7txTVA130_provenance.