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{
"nodes": {
"n1": {
"categories": [
"biolink:Gene"
],
"ids": [
"NCBIGene:7252"
],
"name": "Gene"
},
"n2": {
"categories": [
"biolink:SequenceVariant"
],
"name": "Sequence Variant"
},
"n3": {
"name": "autism",
"categories": [
"biolink:Disease"
],
"ids": [
"MONDO:0005260"
]
}
},
"edges": {
"e0": {
"subject": "n1",
"object": "n2",
"predicates": [
"biolink:related_to"
]
},
"e1": {
"subject": "n2",
"object": "n3",
"predicates": [
"biolink:related_to"
]
}
}
}
This query connects a particular gene to autism via sequence variants.
This query runs against robokopkg and returns 3 results. Running in strider produces 0 results. I did some experiments and it seems like strider is able to get variants, so maybe there is something happening at the NN step? NN doesn't handle sequence variants, but the variant id's coming each direction from robokop should still line up.
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