Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion description "[GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion evidence source_evidence_literature NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion SIO_000772 19567835 NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion wasDerivedFrom gad-20130706 NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_assertion wasGeneratedBy ECO_0000203 NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP87086.RAmMP3MK9Nw15gmT3xBt-sIFWlCxHgcK_Af-NWLn5MilU130_provenance.